373 Concurrent Hemoptysis and Hemothorax: A Life-Threatening Presentation of Pulmonary Sequestration in Adulthood

We have also learned over the ensuing decade that some of these lesions may display dynamic changes in utero. For example, CCAM Type III was once thought to have a uniformly poor prognosis and as a result prenatal diagnosis would often lead to TOP. However, a proportion of cases of CCAM Type III diagnosed prenatally have been shown to resolve spontaneously. The King's College London study reported this dynamic process in 9% of its series, while a large Canadian study recently showed that 56% of cases of CCAM regressed spontaneously7. In contrast, tumor growth and hemodynamic deterioration may complicate clinical management of these lesions. To add to the confusion, the two most common pathologies of the fetal lungs, CCAM and bronchopulmonary sequestration (BPS), which seemed to be pathologically and clinically distinct, frequently overlap8, and confused terms such as 'hybrid form' and 'missing link' appear in the literature9, 10. These new and conflicting data are the tip of the iceberg of conjecture and controversy surrounding the etiology and pathogenesis of fetal lung lesions, and classification of a specific lung anomaly according to traditional criteria has become irrelevant. It is time to revise the terminology of congenital lung lesions, not least in light of emerging in-utero treatment modalities for these malformations11. We review here the latest pathological and pathogenic aspects of fetal CCAM and BPS, in an attempt to draw a parallel with prenatal ultrasound technology. Our aim is to propose a new classification system based on the pathogenesis of these malformations and their two-dimensional (2D) and color Doppler ultrasound characteristics. Elsewhere12 we demonstrate the applicability of this classification system in a clinical setting. Proliferation of polypoid glandular epithelium Proliferation of smooth muscle and elastic tissue in cyst walls Absence of cartilage Absence of inflammation Normal arterial and venous connections. Type I: The lesion has large cysts > 2 cm diameter, frequently producing mediastinal compression. The cysts are lined by ciliated pseudostratified columnar epithelium. The walls of the cysts contain prominent smooth muscle and elastic tissue. Mucus producing cells are present in one-third of cases and cartilage in the wall is rarely seen. Relatively normal alveoli may be seen between the cysts. The prognosis is good. Type II: The lesion contains multiple small cysts < 1 cm diameter, which histologically resemble dilated terminal bronchioles with mixed columnar and cuboidal linings. The area between the cysts is occupied by large, distended, alveolar-like structures. Mucus cells and cartilage are absent and, rarely, striated muscle fibers may be seen. This group has significant associated anomalies, and therefore a poor prognosis. Type III: This malformation was a bulky, non-cystic lesion, typically creating a large, solid mass affecting an entire lobe or lobes and producing mediastinal shift. Histologically the mass is composed of regularly spaced, alveolus-like structures lined by ciliated cuboidal epithelium and separated by masses of alveolus-sized structures lined with non-ciliated cuboidal epithelium. This subgroup also has a very poor prognosis. In a subsequent study Stocker expanded his classification to five types based on the site of origin of the malformation: tracheal, bronchial, bronchiolar, bronchiolar/alveolar duct and alveolar/distal acinar. Each subgroup was labeled '0' to '4', indicating the lesion's progression distally along the airway16. BPS represents a developmental mass of non-functioning bronchopulmonary tissue that is separate from the tracheobronchial tree and receives arterial blood from the systemic circulation, which is pathognomonic for this condition. Pryce was the first to coin the term 'sequestration' (from the Latin, sequestra, to remove or separate) to describe this disconnected bronchopulmonary mass or cyst with an anomalous systemic arterial supply17. The classification of BPS is, however, complicated. Two subtypes were primarily defined: the intralobar mass located within the substance of a lung lobe, and extralobar BPS, which has its own pleural investment. The extralobar subtype can occur in the chest, including the pericardial sac, or in the abdomen, whereas the intralobar subtype is limited to the lung. Subsequently, in 1974 Sade showed that BPS has diverse variant forms, including bronchopulmonary and vascular related malformations. He proposed the term 'sequestration spectrum'. At one end of the spectrum is anomalous blood supply to a normal lung while at the other end is abnormal lung tissue without anomalous vascular supply18. Between these two extremes is a large group of variant BPS that encompasses anomalies ranging from intrapulmonary sequestration to extrapulmonary sequestration with or without gastrointestinal communications, i.e. bronchopulmonary foregut malformations19. Histologically, the extralobar BPS is a cystic or solid mass of lung parenchyma with a high ratio of mesenchyme to air space. A dilated bronchial structure with bronchial epithelium and cartilage without connection to the bronchiole system is seen. Typical to BPS is the appearance of systemic arteries with distinct elastic layers, thick media and collagenous sheaths that do not accompany bronchial structures, unlike normal pulmonary arteries. Intralobar BPS is characterized by ciliated columnar or flat epithelium that may line acquired cysts containing pus or mucus20. Owing to this difference and since it has not been observed in utero or in some neonates21, the intralobar variant is deemed to be an acquired phenomenon. In the fetus, abdominal extralobar BPS may present as a retroperitoneal mass or cyst, which may lie next to the stomach or communicate with it. The arterial supply is nearly always from the descending aorta and therefore represents a persistence of primitive splanchnic arteries that supply the early foregut. Venous drainage is typically through the azygos system or the inferior vena cava; however, in about 25% of cases the venous drainage is through the pulmonary veins22. Approximately 60% of fetuses with extralobar BPS have associated anomalies, including diaphragmatic anomalies (28%), other pulmonary anomalies (10%) and cardiac malformations (8%), while only 14% of patients with intralobar BPS have other associated anomalies23. Intra-abdominal BPS appears in approximately 10% of cases of extralobar BPS, and 90% of them occur on the left side24, 25. More than 60 years following the first report by Chin and Tang13, the pathogenesis of CCAM and BPS is still unclear. Although all lung lesions appear as distinct types, their embryogenesis may overlap significantly26. Various etiologies have been suggested to describe the pathogenesis of CCAM, among them overgrowth13, hyperplasia27 and hamartoma28. However, all agreed that the defect occurred at the level of the bronchiole. Stocker et al.15 were the first to attempt classification of CCAM types based on embryogenesis, or the developmental stage at which the insult may have occurred. According to these authors the absence of bronchial cartilage differentiates CCAM from true bronchogenic cyst and indicates that the insult occurred before the tenth week of gestation. Type I lesion was hypothesized to stem from an insult occurring as late as 49 days postconception, while Type II probably resulted from an insult occurring earlier than 31 days postconception, since these lesions were frequently associated with other severe congenital anomalies. Type III lesions present with a pseudoglandular appearance, which may indicate maldevelopment early in embryogenesis. Ostor and Fortune29 viewed the embryogenesis of the disease differently. They stated that the presence of normal alveoli at the periphery of the lesion, with abnormal growth in the center, implies failure of canalization of the terminal bronchioles and subsequent inability to connect the conducting and respiratory elements. They conclude that the insult probably occurred later in gestation, at as late as 16–20 weeks29. Bronchography studies and serial microscopic examination showed that bronchial atresia is the primary defect leading to the development of CCAM. The morphology of the lesion, i.e. the type of malformation, is determined by the extent of dysplastic lung growth beyond the atretic segment30. Modern pathological studies have suggested that CCAM may arise from failed interaction between mesenchyme and epithelium during development and a lack of maturation. This observation was confirmed by immunohistological studies of CCAM cases that showed discordance between a high epithelial proliferation rate corresponding to that of mature lung, and hypovascularity corresponding to late first-trimester fetuses. Thus the discordance between vascularity and proliferation in CCAM may represent an arrest in vascular development and a loss of synchrony between stroma and epithelium31. It was suggested that in the developing lung the interaction between epithelial cells and interstitial cells is crucial to normal lung development32. The imbalance between cell proliferation and programmed cell death or apoptosis has been demonstrated in CCAM. Examination of the factors involved in cell proliferation and apoptosis can provide insight into the pathogenesis of CCAM. Some tissue growth factors have been studied as possible mediators for increased cell proliferation in CCAM. Keratinocyte growth factor was not found to mediate increased proliferation33, however glial cell-derived neurotrophic factor (GDNF) seemed to be correlated with epithelial cell proliferation while no GDNF expression was demonstrated in the stromal component of CCAM34. Similarly, greater expression of the proliferation factor, platelet-derived growth factor BB, was found in fetal CCAM than in age-matched normal fetal lung35. The role of apoptosis in CCAM was also analyzed. CCAM lesions requiring resection before birth had a five-fold lower apoptotic index when compared with age-matched normal fetal lung35. It can be summarized that focal asynchrony between epithelial and vascular development in CCAM leads to this congenital maldevelopment. Investigation of other factors that down-regulate apoptosis or up-regulate proliferation in CCAM may further illuminate the pathogenesis of this entity. The pathogenesis of BPS is much more obscure than that of CCAM, and many theories have been proposed36. One states that failure of the pulmonary artery to develop fast enough to supply the whole of the growing lung leads to persistence of the embryonal systemic aortic supply. The lung area so supplied may undergo cystic and fibrous degeneration. Other authors hypothesized that insufficient pulmonary arterial blood supply may be related to the presence of systemic pulmonary collaterals22. Although some authors attempted to view the pathogenesis of BPS as distinct from that of CCAM, they appear to have similar causes. The mechanism of their development has been described as a continuum of anomalous interactions among adjacent cells' excreted factors, to explain the overlap between them26. The microscopic resemblance of BPS and CCAM, which consists of immature or dysplastic lung tissue and the absence or reduced number of bronchial cartilage plates37, and the frequent appearance of CCAM receiving systemic arterial blood supply, indicates a common primary defect early during embryogenesis38. The most prevalent theory states that during early development the laryngotracheal groove arises as a ventral out-pouching of the primitive foregut and migrates caudally to give rise to the bronchial tree. It is possible that in the early stages of development, when the lung bud lies in close proximity to the primitive foregut from which it is derived, some insult or adhesion in an area where these two developing organ systems are adjacent will affect both structures, resulting in a lung lesion and foregut malformation39. The observation that BPS encompasses a great variety of anomalies known also as bronchopulmonary foregut malformation and neuroenteric malformations confirms further the 'sequestration spectrum'. The frequent association of BPS with diaphragmatic hernia, gastric duplication, esophageal fistula and neuroenteric lesions supports the notion that the defect occurs early in organogenesis40. Prenatal diagnosis of fetal lung lesions relies on the appearance of space-occupying lesions or the appearance of chest masses41. Fetal lung lesions must be differentiated from congenital diaphragmatic hernia, which is diagnosed if intrathoracic stomach or bowel loops are identified. The appearance of fetal CCAM varies from predominantly solid to purely cystic masses, while BPS appears as a well-circumscribed, uniformly echogenic solid mass, usually found in the left basal thorax42. Doppler ultrasound technology can be very useful in distinguishing between CCAM and BPS: the latter is supplied by a supporting systemic artery arising from the abdominal aorta, while CCAM is supplied by the pulmonary artery43. Intra-abdominal extrapulmonary sequestration is usually identified in the upper left abdomen as an echogenic mass, most often situated beyond the stomach. The differential diagnosis includes suprarenal masses, however the demonstration of a systemic feeding artery confirms the diagnosis of BPS. Early reports on fetal lung lesions adopted the Stocker system for in-utero classification. The purpose of precise in-utero definition of fetal lung lesions is to extrapolate prognosis. Although the Stocker system was the most widely used, some major drawbacks were recognized. First, it is based on histological criteria, which cannot be applied to prenatal ultrasound technology. Second, Stocker's prognoses and outcomes were derived from the clinical data and features of 38 neonates collected from 1917 to 1975, and are no longer pertinent. In view of these disadvantages Adzick et al.44 suggested abandoning Stocker's three types and dividing CCAM into two major groups based on gross anatomy and ultrasound. The two categories were based on the predominant component of the lesion (cystic or solid): the macrocystic group contains single or multiple cysts ≥ 5 mm diameter, while the microcystic tumors are more solid and bulky with cysts < 5 mm diameter. The idea of subtyping CCAM into two main groups according to the predominant lesion was not new and had been suggested previously by Ostor and Fortune29 and Bale45. The variants are readily differentiated on prenatal ultrasound because the macrocystic type appears as fluid-filled lesions, whereas the microcystic lesions have innumerable interfaces that return the ultrasound beam and therefore appear solid. This simple classification into two types has become the gold standard of in-utero CCAM diagnosis46. Since the original report by Adzick et al.44, numerous studies of the outcome and natural history of fetal lung lesions have been published47-49. However, the main problem with the current classification system is that it relies on a dichotomous definition of the lung anomaly either as CCAM or as BPS. Although the prenatal diagnosis of lung lesions is simple and Doppler studies have enhanced our ability to identify BPS, defining the exact nature of the anomaly may still prove difficult. BPS may have a sonographic appearance similar to that of CCAM (Figure 1), particularly in the microcystic subgroup. Moreover, whereas in the past histological features of CCAM had rarely been reported in BPS, no clear histological distinction exists between these two entities, and mixed histopathological findings of typical CCAM can be seen even in bronchial and laryngeal atresia50. Cystic lesions with the clinical appearance of CCAM may have systemic blood supply and BPS may have a histological appearance similar to CCAM51-53. (a) Ultrasonographic image showing a prominent left echogenic lung interpreted as microcystic congenital cystic adenomatoid malformation with a hypoechoic line of unknown origin. (b) A color Doppler image demonstrates the prominent arteriovenous shunt. The Doppler study established the diagnosis as bronchopulmonary sequestration. Recently a large pathological study found histological features compatible with CCAM Type II in approximately 50% of the cases with proven extralobar BPS. This study also showed that 11/12 (91%) prenatally diagnosed BPS cases demonstrated elements of CCAM; the authors concluded that the occurrence of CCAM in BPS is more frequent than reported in the literature8. Cass et al.9 suggested the term 'hybrid form' to describe six cases of BPS in which the histological features were similar to those of CCAM. These findings suggest a common developmental link between BPS and CCAM10. These accumulated data regarding the exact definition of fetal lung lesions make prenatal counseling very difficult and postnatal management uncertain54, particularly since prognosis is related to lesion classification, and those with supposed poor prognosis (the microcystic group) may resolve spontaneously in utero47, 48, 55. As has been discussed, congenital malformations of the lung are an ill-defined group of lesions. The present state of our knowledge on fetal lung masses indicates that the traditional classification of BPS and CCAM is insufficient to provide definitive information regarding the pathogenesis and prognosis in each individual case. Since in many instances the clinical and morphological features of both CCAM and BPS show considerable overlap, a unifying concept of their pathogenesis and classification was proposed. In 1969, Culiner proposed viewing the three entities, i.e. congenital bronchial cystic disease, sequestration and congenital bronchiectasis, as a variant of a single primary complex of bronchovascular anomalies56. Buntain et al. later suggested that all congenital lung lesions should be considered as one clinical group57. Demos and Teresi58 suggested in 1975 grouping the possible etiologies for congenital lung malformations. Heitzman stated still further that although the terminology of congenital lung malformations suggested that these are discrete entities, their morphological characteristics overlap, thus supporting the notion that they stem from a common embryological event59. Until the late 1980s, no concerted attempt was made to clarify the pathogenesis or classification of congenital lung lesions; most classification systems in the medical literature were based on histological findings15, 16. Clements and Warner60 were the first to suggest a model, based on original research, centered on a rational sequence of events in lung development, known as the 'wheel' theory. This model helped elucidate and simplify the classification of congenital lung anomalies. The authors based their theory on the assumption that any insult to the tip of a developing bronchus may lead to a different lesion depending on the timing and severity, rather than on the nature, of the insult. According to Clements and Warner the terms intralobar, extralobar, sequestration and CCAM provide no definite information on the morphology within these lesions. They were the first to suggest considering all anatomical components of the lung involved in the pathological lesion in each particular case. These components are the bronchial airways, the arterial supply and venous drainage, and the lung parenchyma. In a subsequent study the authors confirmed the applicability of this approach on 25 neonates with bronchopulmonary vascular malformations61. With the advent of high-resolution ultrasound technology, coupled with sophisticated Doppler and power Doppler angiography, it is now possible to evaluate fetal arterial62 and venous systems63. We therefore adopted Clements and Warner's classification system with modifications, based on 2D and Doppler ultrasound, and applied it to fetal findings. Clements and Warner60 originally proposed the term 'malinosculation' (from the Latin: mal, abnormal; in, in; osculum, mouth) to describe the various anatomical combinations. However, this term failed to gain general acceptance. We prefer the term dysplasia64 (from the Greek: dis, abnormal; plasis, forming), meaning abnormal tissue formation. We believe the term dysplasia more aptly describes the abnormal development of lung tissue involved in this group of anomalies. Agenesis of the lung: includes the most severe dysplasias, wherein the insult is sufficiently early and proximal to the bronchial bud to arrest lung, lobe or lobule development ('wheel' theory Type I). Normal lung with abnormal vascular supply: the bronchial tree continues to develop normally, but pulmonary artery growth is arrested, resulting in normal lung with an isolated segment supplied by persistent systemic vessels instead of the pulmonary artery ('wheel' theory Type III). Abnormal lung with abnormal vascular supply: this includes the 'classic' form of BPS, with disruption to both the airway tract and pulmonary arterial development resulting in systemic arterial supply to abnormal lung parenchyma ('wheel' theory Type IV). Abnormal lung with normal vascular supply: this category includes bronchogenic cysts and 'classic' CCAM ('wheel' theory Types II, V). Miscellaneous: includes laryngeal atresia with bilateral echogenic lung, split notochord syndrome or bronchopulmonary dysplasia with neuroenteric association. The novelty of our new classification system is that it enables separate delineation of each fetal lung component involved in the anomaly: the parenchyma, arterial circulation and venous drainage. Further, it is based on prenatal sonographic identification and Doppler flow studies: the arterial supply and venous drainage of the lesions, as opposed to tissue consistency. In the past, polyhydramnios, mediastinal shift and tumor size were considered bad prognostic factors in fetuses with lung lesions5-7. However, all previous studies ignored the lesions' vascular component in their evaluation. We believe that the morphologic description of the lesion as solid or cystic does not affect fetal prognosis, since the natural course of the entity during gestation is probably influenced primarily by the vascular component of the malformation. The pivotal role of vascular assessment was demonstrated by Clements et al. in their clinical study61 and recently verified in a further original study65. The appearance of hydrops fetalis was shown to be the only significant poor prognostic factor in fetuses affected with lung abnormalities5-7, 44, 46. Several possible mechanisms for the development of hydrops fetalis have been suggested. It was postulated that hydrops may be secondary to caval obstruction or cardiac compression from large tumors causing mediastinal shift66. This theory has never been verified, and is in fact contradicted by the finding that severe cases of lung anomaly with diaphragmatic hernia do not develop hydrops, despite significant intrathoracic mass. Other theories have proposed a vascular etiology for hydrops development. Some suggest that overcirculation through the sequestrated lung may induce congestive heart failure with resulting hydrops67, while others have raised the possibility of twisting of the vascular resulting in obstruction of the venous and The latter has recently been verified in a arterial of the of a systemic artery to of lung The authors postulated that venous obstruction the seen on prenatal ultrasound, probably as a result of blood into the interstitial space. Similarly, it can be that the in utero of fetal lung may be to such lung overcirculation may also result from occurring with gestation. In our clinical we demonstrate the of hemodynamic in two neonates through arterial and the of fetal with We believe that with ultrasound and sophisticated Doppler in-utero of related vascular anomalies in fetuses with lung dysplasia is now of significant intrapulmonary and vascular may provide of the pathogenesis of these lesions and prenatal It is that in-utero to hemodynamic deterioration of fetuses with lung lesions be The pathogenesis and in-utero classification of fetal lung lesions should be The proposed of the lung according to the by of each lung component involved in the lesion, will classification of fetal lung anomalies. We believe that this simple approach based on 2D and Doppler of vascular anomalies will further our of the of fetal lung lesions. The applicability of this new classification system to clinical management is in the

Cystic lung lesions with systemic arterial blood supply: A hybrid of congenital cystic adenomatoid malformation and bronchopulmonary sequestration

Pulmonary sequestration presenting as a massive haemoptysis in adult: A case report

Paediatric torsed extralobar sequestration containing calcification: Imaging findings with pathological correlation

We present a case of a young adult patient with haemoptysis and back pain following 2 days of worsening cough. CT imaging revealed an intralobar pulmonary sequestration of the left lower lobe with an anomalous arterial supply from the thoracic aorta and a large associated haemothorax. The patient developed haemodynamic instability and was taken emergently to the operating room for left thoracotomy. Intraoperatively, active haemorrhage from the aberrant systemic vessel was identified, controlled and ligated. A left lower lobectomy was performed, and the patient made an excellent recovery.Pulmonary sequestration is a rare congenital anomaly of non-functioning lung parenchyma with systemic arterial supply, typically presenting in childhood with recurrent infections. Rarely, as in this case, it presents in adulthood with life-threatening haemorrhage. This case underscores the importance of early recognition and prompt surgical management in adult presentations of pulmonary sequestration with haemorrhagic complications.

A sword threatening the heart: The scimitar syndrome

Pulmonary sequestration is a rare congenital malformation of lung in which a part of the lung is supplied by an anomalous systemic blood supply from thoracic or abdominal aorta. This is a nonfunctioning lung tissue and lacks normal communication with tracheobronchial tree. It develops from accessory lung bud. If developed before pleura formation, it results in intralobar sequestration, and extralobar, if it develops after pleura formation. Usually Intralobar type of pulmonary sequestration presents in late childhood or adolescence with recurrent pulmonary infections. It is less commonly associated with foregut communication or associated anomalies, unlike the latter. Extra lobar type usually presents with respiratory distress while recurrent infections are less common. In the present case report a 76-year-old male patient was diagnosed with intralobar pulmonary sequestration. This patient was presented with recurrent respiratory infections with complaints of fever and cough with expectoration for one week. Previously the patient was misdiagnosed with recurrent pneumonia. Despite the age of patient, consideration of pulmonary sequestration as a differential diagnosis lead to investigations in that direction. This helped in prompt diagnosis and further plan of management. Misdiagnosis of this condition may have lead to development of complications like recurrent infections and abscess. These complications can be avoided by prompt surgical excisions which are curative. This case report was unique because it diagnosed pulmonary sequestration in a 76 years old patient who presented with recurrent pneumonia.

We report the case of a fit and healthy 41-year-old man, who presented with significant haemoptysis without a history of recurrent infections. His computed tomography scan showed a dense lesion in the left lower lobe with a feeding vessel arising from the abdominal aorta, characteristic for an intra-pulmonary sequestration. To prevent possible further haemoptysis or infections, a left lower lobectomy was performed. The histological examination showed the typical features of a sequestration. However, within the sequestration, a carcinoid tumour without atypical features was found. There was no lymph node involvement. Sequestrations are congenital lesions without communication with the bronchial tree and with a systemic blood supply. They commonly cause recurrent infection. Fatal haemoptysis has also been described, but is rare. There are very few reports of neoplastic lesions in sequestrations. This case illustrates two unusual aspects of sequestrations. Surgery offers definitive treatment for both pathologies, as opposed to embolisation.

A LUNG WITHIN A LUNG? A CASE REPORT OF MASSIVE HEMOPTYSIS SECONDARY TO PULMONARY SEQUESTRATION

Background: Pulmonary sequestration is a rare congenital anomaly involving non-functional lung tissue with systemic arterial blood supply. Its implications for pediatric growth and weight are poorly documented. Case report: An 8-years-and-10-month-old previously healthy boy was diagnosed with pulmonary sequestration following pneumonia. Chest imaging revealed emphysematous changes, and computed tomography confirmed intralobar sequestration. Surgical removal was performed, revealing significant growth impairment with weight (18.9 kg) and height (117 cm), both below the 3rd percentile at admission, despite normal laboratory findings. Discussion: Pulmonary sequestration can negatively influence pediatric growth due to chronic inflammation and hypoxia from recurrent infection. Surgical intervention typically results in clinical improvement and significant catch-up growth. Conclusion: This case highlights pulmonary sequestration’s potential negative impact on pediatric growth and underscores the importance of early surgical intervention for improving growth outcomes.

1. William T. Scouten, MD* 2. Jeanette White, MD† 1. *National Capital Consortium Pediatric Residency Program, National Naval Medical Center/Walter Reed Army Medical Center, Washington, DC 2. †Pediatric Critical Care, Children’s National Medical Center, Washington, DC A previously healthy 17-year-old girl complains of a “dry and intermittent” cough for the past 1.5 months. The cough worsens when she is recumbent and does not respond to over-the-counter cough medications. The cough is not associated with fever, chills, nausea, vomiting, night sweats, or weight loss. She reports several episodes of posttussive chest pain. Recently prescribed treatments of albuterol and fexofenadine do not alleviate her symptoms, despite her clinical diagnoses of exercise-induced bronchospasm and allergic rhinitis. She is an accomplished basketball player; her cough does not diminish her athletic performance. The patient’s past medical history is remarkable for a cardiac murmur noted at birth that resolved by 2 years of age and for three episodes of pneumonia by 6 months of age. She has no drug or environmental allergies, her immunizations are up-to-date, and her growth and development are normal. She denies drug, alcohol, or tobacco use. Further review of a psychosocial history reveals minimal adolescent risk characteristics. For the past 6 years, she has lived in the southwest United States and spent the prior summer in northern California. She denies exposure to others who had chronic cough, tuberculosis, or lung diseases. She admits to watching bats on one occasion during vacation in the past year. On physical examination, the patient appears healthy and is in no apparent distress. Vital signs are: temperature, 36.8°C (98.2°F); respiratory rate, 22 breaths/min; pulse, 88 beats/min; blood pressure, 117/73 mm Hg; and pulse oximetry, 100% hemoglobin-oxygen saturation while breathing room air. The patient’s respirations are unlabored, and she has adequate air movement. Auscultation of the chest reveals decreased breath sounds over the left base and fine, end-inspiratory crackles within the midposterior left chest. There is no appreciable egophony. The remainder of the physical findings are normal. A complete blood count reveals a white …

CARCINOID TUMOR IDENTIFIED WITHIN A SEQUESTERED LUNG

A Rare Anatomical Variant of Pulmonary Sequestration

Contrast computer tomography (CT) scanning is the investigation of choice for the further assessment of suspected cystic congenital lung lesions (CCLL). Its use to identify the presence of anomalous feeding vessels supplying the lesion is well documented, but data regarding its accuracy is limited. This study compares CT results to operative and pathological findings to determine the accuracy of CT in identifying these anomalous vessels. 51 consecutive cases of cystic congenital lung lesions managed in one hospital by a single consultant were reviewed. All cases had contrast CT scans performed preoperatively, as standard practice in this institution. We compared the results of these CT scans to the macroscopic appearance at surgery and histological findings postoperatively. We also compared the results of 2 CT protocols used in our institution between 1999-2007 and 2007-2009, respectively. Anomalous vessels were reported on CT in 9 cases. All but 1 had concordant operative and pathological findings. In the remaining 42 cases, no anomalous vessels were seen on CT. Of these, 9 cases were found to have an anomalous blood supply at surgery, 6 of which were hybrid lesions and 3 isolated sequestrations. The specificity of CT in identifying feeding vessels in the study was 97% (95% CI: 0.83-0.99) and the sensitivity was 47% (95% CI: 0.23-0.71). The positive predictive value was 89% (95% CI: 0.50-0.99) and negative predictive value 79% (95% CI: 0.62-0.89). The most recent protocol yielded an improved sensitivity of 75% (95% CI: 0.22-0.98) and a specificity of 100% (95% CI: 0.46-1.0) with a 100% (95% CI: 0.31-1.0) positive and 83% (95% CI: 0.36-0.99) negative predictive value. CT is a specific investigation for identifying anomalous vessels in CCLL but lacks sensitivity, leading to a relatively low negative predictive value. This emphasises the need in every case to look for anomalous vessels at surgery to avoid morbidity and potential mortality. An improved protocol for CT scans leads to improved specificity and sensitivity and predictive values.

BackgroundPulmonary sequestration is a rare congenital lung anomaly, presenting mostly in childhood and adolescence.Case presentationWe report the case of a 26-year-old male patient presenting with pleuritic left sided chest pain and haemoptysis. Computed tomography of the chest showed features of intralobar pulmonary sequestration involving the left lower lobe, with arterial supply arising from the descending thoracic aorta above the diaphragm and normal venous drainage. Video assisted thoracic surgery was planned to perform a left lower lobectomy. Considering the risk of bleeding from the large artery supplying the sequestered segment, a posterolateral thoracotomy incision was made and left lower lobectomy was completed, with successful division of the arterial feeder. The patient was discharged home without complications. Pathologic examination of the specimen grossly revealed partial division of the lobe by two fissures with extensive adhesions into an upper and lower portion with no clear demarcation and a large vessel which enters the lower portion at the posterior inferior aspect, separate from the hilum with a diameter 10 mm. Microscopically, both portions of the lobe showed normally alveolated lung tissue with patchy recent intra-alveolar haemorrhage and evidence of chronic inflammation in the sequestered segment. There was no evidence of malignancy.ConclusionThis case highlights the rare presentation of pulmonary sequestration in adulthood and the importance of imaging to identify anomalous arterial supply to the sequestered segment in the left lower lobe of the lung. The use of safe surgical techniques to control the anomalous systemic arterial feeding vessel cannot be overemphasized.