The College of American Pathologists offers these protocols to assist pathologists in providing clinically useful and relevant information when reporting results of surgical specimen examinations. The College regards the reporting elements in the “Surgical Pathology Cancer Case Summary (Checklist)” portion of the protocols as essential elements of the pathology report. However, the manner in which these elements are reported is at the discretion of each specific pathologist, taking into account clinician preferences, institutional policies, and individual practice.The College developed these protocols as an educational tool to assist pathologists in the useful reporting of relevant information. It did not issue the protocols for use in litigation, reimbursement, or other contexts. Nevertheless, the College recognizes that the protocols might be used by hospitals, attorneys, payers, and others. Indeed, effective January 1, 2004, the Commission on Cancer of the American College of Surgeons mandated the use of the checklist elements of the protocols as part of its Cancer Program Standards for Approved Cancer Programs. Therefore, it becomes even more important for pathologists to familiarize themselves with these documents. At the same time, the College cautions that use of the protocols other than for their intended educational purpose may involve additional considerations that are beyond the scope of these documents.This protocol applies to germ cell tumors located in the mediastinum, sacrococcygeal area, retroperitoneum, neck, and intracranial sites. There is no American Joint Committee on Cancer (AJCC)/International Union Against Cancer (UICC) TNM staging system for the staging of extragonadal germ cell tumors. The Children's Oncology Group Staging System is recommended.Extragonadal Germ Cell Tumor: ResectionSelect a Single Response Unless Otherwise Indicated* Data elements with asterisks are not required. However, these elements may be clinically important but are not yet validated or regularly used in patient management.Patient Age (note A)*Specimen IntegrityTumor Site (note B)Tumor Size (note C)Tumor WeightHistologic Type (select all that apply) (note D)TeratomatousNonteratomatous*Histologic Grade (applicable to immature teratomas only) (note E)Microscopic Tumor Extension (applicable to sacrococcygeal tumors only)Margins (select all that apply) (note F)*Treatment Effect*Lymph-Vascular Invasion (note F)*Perineural InvasionRegional Lymph NodesDistant MetastasisPathologic Staging (select all that apply) (note G)Children's Oncology Group Staging for any Malignant Extragonadal Germ Cell Tumors (see also specific staging systems for sacrococcygeal and mediastinal germ cell tumors)*Anatomic Classification of Sacrococcygeal Germ Cell Tumors*Moran and Suster Proposed Clinical Staging for Mediastinal Germ Cell Tumors†† Applies to adult (postpubertal) extragonadal germ cell tumors.*Additional Clinical or Laboratory Findings (select all that apply)*Comment(s): ______________________________________A: Patient Age.—The behavior of pediatric and adult extragonadal germ cell tumors (EGCTs) is quite distinct. As outlined below, within the pediatric age range, prognosis is worse with increasing age. Most studies of pediatric EGCTs include both neonates and older children, making it difficult to discern the precise pathology and clinical course of EGCTs in the older child.1–5 A recent study6 has suggested that age 12 years or older is a significantly adverse prognostic factor, especially for thoracic tumors and, therefore, may represent the transition point to adult type tumors.The notes that follow are divided into congenital/neonatal EGCTs (birth to 6 months) and childhood/prepubertal germ cell tumors (GCTs) (7 months to approximately 12 years) because of the well-documented differences in their pathology and prognosis. Postpubertal/adult EGCTs are defined as occurring in patients 12 years and older.These notes describe important differences in the pathologic diagnosis and prognosis of EGCTs in different age groups: congenital/neonatal, children (prepubertal), and adult (postpubertal). They are summarized in the Table. Within each age group, the significance of anatomic site and morphologic subtyping is emphasized. Other issues discussed include postchemotherapy evaluation, unique associated malignancies, and associated syndromes. Finally, discussion of differential diagnoses is presented based on anatomic location and patient age.B: Site.—Congenital/Neonatal.—Other than direct effects on local vital organs, the behavior of congenital and neonatal GCTs seems to be independent of anatomic location.6–9 Sacrococcygeal teratomas are the most common GCT of the neonate, occurring more frequently in girls.10 After intracranial teratomas, other more-common sites of neonatal teratoma include the mediastinum (pericardium, heart, thymus, and lung), head and neck region (including thyroid), and the retroperitoneum.6,7,9,11,12 Neonatal teratomas may occur anywhere along the body midline, following the course of the embryonic germ cell ridge. These tumors have a similar morphology at each site.In one published study13 of 534 fetal and neonatal GCTs, sacrococcygeal teratoma was the leading teratoma (214; 40%). Next were intracranial (71; 13.3%) and cervical (70; 13.1%) teratomas, followed by palatal and nasopharyngeal (41; 8%), cardiac (40; 7.5%), gastric (14; 2.6%), mediastinal (13; 2.6%), orbital (13; 2.4%), facial (8; 1.5%), and placental (8; 1.5%) teratomas. There were 17 miscellaneous teratomas (3%), variously located in the tongue, tonsil, liver, retroperitoneum, eye, mesentery, ileum, testis, vulva, and anorectal area. In addition, 25 examples of fetus in fetu were identified.Mediastinal GCTs occur more commonly in the older adolescent and postpubertal child. Mixed-malignant GCTs comprising teratomas, yolk sac tumors, embryonal carcinomas, and rarely, choriocarcinomas are more frequent with increasing age. Germinoma is generally not seen in children younger than 10 years.14 As in congenital teratoma, the prognosis of mediastinal GCTs in children is significantly affected by tumor stage and completeness of surgical excision (see notes F and G).15 Rarely, sarcomatous elements are reported in pediatric mediastinal GCTs.16Sacrococcygeal tumors in the older infant and child are predominantly presacral and pelvic, with no externalized mass noted at birth. Malignancy rates are reportedly very high in these children, most commonly from yolk sac tumors.12,17 It is thought that many of these tumors represent congenital sacrococcygeal GCTs (SGCTs) with an overgrowth of yolk sac tumor, analogous to the malignant recurrences of yolk sac tumors in children with incompletely excised congenital SGCTs.12,18Although pelvic and/or retroperitoneal extension of a sacrococcygeal tumor is not unusual, an exclusively retroperitoneal or abdominal location is uncommon, comprising less than 5% of all EGCTs.Most intracranial germ cell tumors arise in structures around the third ventricle, most commonly in the pineal gland or suprasellar region. Other sites include intraventricular, basal ganglionic, thalamic, cerebral hemispheric, bulbar, intramedullary, and intrasellar. Most occur in the second decade of life, with approximately one-quarter of all central nervous system germ cell tumors arising in the prepubertal years.19 The most common subtype is germinoma, followed by teratoma.20The mediastinum is the most common anatomic site for extragonadal GCTs in adults. These tumors are overwhelmingly restricted to males, but well-documented cases in women do exist.21–22 The histologic classification of GCTs at this site is identical to that used in the gonads: seminomatous (pure), nonseminomatous (yolk sac tumor, embryonal carcinoma, choriocarcinoma, and mixed GCTs), and teratomas. One important difference is that, unlike the situation in the adult testis or in congenital/pediatric GCT, the distinction between mature and immature teratoma is important in the adult mediastinum.Sacrococcygeal GCTs in this age group are generally considered to have been present since birth. In some cases, there is a history of a partially resected neonatal lesion to support this interpretation. The location is similar to that seen in pediatric cases, except that most are intrapelvic because tumors with an external component would be expected to have been discovered in childhood. Adenocarcinoma may arise in the SGCT of adults.23The distribution of cervical GCTs (CGCTs) in adults is similar to that seen in children, with frequent involvement of the thyroid. Some cases have presented in continuity with a mediastinal GCT.Most purely retroperitoneal GCTs in adults represent metastases from an undiscovered or occult primary tumor in the testicle or, rarely, in the ovary. In general, a testicular primary must be excluded clinically.Intracranial germ cell tumors are more common in the postpubertal child and younger adult, with the anatomic location as described above.C: Tumor Size.—The number of sections submitted varies with the size and character of the specimen and the nature of the underlying neoplastic process. At least 1 section per centimeter of the tumor's greatest diameter is recommended if the tumor is a germ cell neoplasm because diverse elements may only be found in this way and might affect the tumor classification.24Large SGCT may be associated with fetal hydrops because of increased demands on the heart to supply the tumor vasculature and may be associated with fatal intratumoral hemorrhage with delivery. Survival with cervical teratoma depends on the size of the tumor and extent of tissue involvement, with respiratory compromise being the main cause of subsequent morbidity and mortality.11 Neonates with cervical teratomas generally have a good outcome when the tumor is resectable. Fetuses have a much lower survival rate than neonates (23% versus 85%). Ten percent of the fetuses are stillborn.Some epignathi and nasopharyngeal teratomas are so large and extensive that they are incompatible with life and, therefore, inoperable, which explains the high mortality rate.25 The most common presenting findings in these cases are a mass, respiratory distress, polyhydramnios, and dysphagia.13Because of the size of some intracranial teratomas, identifiable anatomic landmarks are lost, making it practically impossible to determine the exact site of origin.13 The anatomic location of the teratoma cannot be determined in about one-third of the patients because the brain is replaced by tumor. When a point of origin can be found, the cerebral hemisphere is the most common primary site, followed by the third ventricle and the pineal region. Large tumors erode through the skull and extend into the orbit, oral cavity, or the neck. Spontaneous rupture during delivery of a fetal head enlarged by tumor has been reported.26D: Histologic Type.—The World Health Organization (WHO) classification of germ cell tumors is the basis for most contemporary classifications and is the one generally used for EGCTs.27 According to this classification, germ cell neoplasms are divided roughly into 7 histologic categories: dysgerminoma, yolk sac tumor, embryonal carcinoma, polyembryoma, choriocarcinoma, teratoma, and gonadoblastoma.27 Gonadoblastoma, a neoplasm typically found in dysgenetic gonads, is included in the category of germ cell tumors (mixed germ cell, sex cord–stromal tumors). According to this classification, fetus in fetu is regarded as a form of mature teratoma. The most common germ cell tumors occurring in the perinatal period in order of rank are teratoma, yolk sac tumor, choriocarcinoma, and gonadoblastoma.Extragonadal germ cell neoplasms can be classified for histopathology using mediastinal nomenclature (ie, teratomatous and nonteratomatous lesions).28Most germ cell tumors of the fetus and neonate are histologically benign and are classified as either mature or immature teratomas.13 Yolk sac tumor (endodermal sinus tumor) is the leading malignant germ cell tumor of the perinatal period and throughout childhood. In the fetus and neonate, it occurs most often with a teratoma and adversely affects the prognosis.The sacrococcygeal area is the location associated with the highest incidence of malignancy, in the form of a yolk sac tumor. The overall frequency of neonatal sacrococcygeal teratomas with a yolk sac tumor is approximately 10%. The values cited in the literature range from 2.5% to 25%.13,29 The presence of immature neuroglial elements in a neonatal teratoma, although worrisome, has no bearing on prognosis, and generally these patients have a favorable outcome. It is well known that an important relationship exists between the age at diagnosis of a patient with a sacrococcygeal teratoma and outcome. The incidence of malignancy in the neonate is approximately 10%, approaching almost 100% by 3 years.13,29–31Congenital teratomas are commonly immature and often contain an admixed yolk sac tumor and, rarely, embryonal carcinoma. In the neonate, the diagnosis of an immature teratoma is is routinely based on the presence of immature neuroepithelium. Choriocarcinoma may be seen as a metastasis from the placenta in the infant but is not reported as a component of primary extracranial EGCTs of childhood.32 Similarly, the presence of germinoma in a congenital teratoma would be very unusual.The occurrence of admixed yolk sac tumor or recurrence as yolk sac tumor is more common with the presentation of teratoma in patients older than 6 months. Similarly, in older infants (after 7 months), the incidence of teratoma falls, whereas the incidence of pure yolk sac tumor increases. Most yolk sac tumors are diagnosed between 7 months and the third year of life. Pure embryonal carcinomas are rare before 5 years old.14 As noted, prognosis worsens with increasing age, and the prognosis (ie, recurrence rate) of completely resected EGCTs worsens at approximately 7 months. The designation of a child as prepubertal is sometimes difficult, but at least one study6 suggests 12 years or older is a significant age boundary.Approximately 43% of all mediastinal GCTs contain teratoma and include mature teratoma (63%), immature teratoma (4%), and teratoma with other malignant components (ie, sarcoma, other malignant germ cell element, or carcinoma) (33%).28 Because histologically mature mediastinal teratomas behave in a clinically benign fashion, regardless of patient age, and immature teratomas have the potential for aggressive behavior, the distinction is critical to patient management in adults. Mature teratomas are histologically similar to those occurring in the ovary. Despite their similarity to ovarian GCTs, monodermal teratomas, such as struma ovarii, have not been described in the mediastinum.In adults, the most common nonteratomatous component is seminoma, but yolk sac tumor, embryonal carcinoma, and choriocarcinoma may also occur. Mediastinal seminoma frequently involves the thymus, with resultant cyst formation and thymic epithelial cell hyperplasia.33 This may make the recognition of the seminomatous component difficult. A high level of suspicion is necessary in the case of cystic lesions of the thymus, especially if associated with a granulomatous response. The morphology of nonteratomatous components is otherwise identical to those in the gonads and will not be repeated here because it has been reviewed in detail elsewhere.34 All nonteratomatous elements should be regarded as malignant in adults.In most SGCTs in adults with adequate descriptions or illustrations, the histology of the germ cell component is that of a mature teratoma, which is benign, if it is pure. Several cases are reported as “malignant teratoma” without further description or illustration. Specific diagnoses and clear descriptions or illustrations do reveal the existence of rare cases of nonteratomatous GCTs, including dysgerminoma, yolk sac tumor, and embryonal carcinoma.35,36 When follow-up is provided, these tumors exhibit the expected malignant behavior.Cervical GCTs are quite rare in adults but have been described with a variety of histologic patterns. Mature teratomas may occur at this site and, when pure, have a uniformly benign behavior.36–40 Nonteratomatous GCTs, including embryonal carcinoma and yolk sac tumor, have been described.41,42 The few reports of non–germ cell neoplasms arising in CGCT include carcinomas43,44 and, possibly, chondrosarcoma.41 Too few of such cases have been described to make generalizations about their behavior, but they would be expected to be aggressive, based on reports from other sites (see note J).E: Grade (Immature Teratomas).—The histologic grade of the tumor is based on 3 factors: degree of immaturity, presence of a neuroepithelial component, and the quantity of the latter.45Grade 1 is given to neoplasms with some immaturity, but with neuroepithelium absent or limited to a rare, low-power magnification (×40) field within the tumor, and not more than 1 such focus in any slide.Grade 2 is given when immaturity and neuroepithelium were present to a greater degree than in grade 1. Neuroepithelium is common but does not exceed 3 low-power microscopic fields in any 1 slide.Grade 3 is given when immaturity and neuroepithelium were prominent, the latter occupying 4 or more low-magnification microscopic fields within individual sections.The presence or grade of immaturity, as defined by Norris et al45 for ovarian teratomas, is not predictive of malignant behavior in congenital EGCTs, although immature teratomas are more likely to have admixed yolk sac tumor. It is well recognized that incomplete surgical resection of neonatal teratomas is associated with recurrences of a pure yolk sac tumor, as seen in cases of sacrococcygeal teratoma for which coccygectomy was not performed.8,24,46,47 In some cases with recurrence, foci of the yolk sac tumor could not be identified in the original resected teratoma.8,24 It is unclear whether that is due to incomplete sampling of the original lesion or whether elements of a residual, immature teratoma can give rise to a yolk sac tumor.Increased patient age, sacrococcygeal location, and grade 2 to 3 immaturity are more frequently associated with admixed yolk sac tumor.46Mediastinal immature teratomas, like their testicular counterparts, are most commonly identified by cellular spindled stroma (ie, immature mesenchyme) surrounding glandular epithelium. Immature neuroepithelial elements, similar to those seen in immature teratomas of the ovary, may also be identified. Immature neuroepithelium should be distinguished from mature ependyma, a relatively common finding in mature teratomas. Other admixed immature elements frequently include cartilage and glandular epithelium, but the diagnosis of immaturity does not typically depend on these elements. At present, there is no grading schema for extragonadal immature teratomas; however, it is reasonable to report the percentage of immature elements.In SGCTs, the existence of an immature teratoma in the absence of a nonteratomatous component seems to be quite infrequent because it is only rarely described.48 The significance of immature tissues is not clear, but we are not aware of a documented case of aggressive behavior.Immature cervical teratomas demonstrate malignant behavior,49–52 similar to those arising in the mediastinum, but unlike those of other extragonadal sites. In some cases, the immature component is described as predominantly neural.Patients with malignant EGCTs (especially adults) often receive cisplatin-based chemotherapy before surgical resection. This clinical practice places an extreme importance on the initial biopsy interpretation and also creates challenges in the evaluation of the resection specimen. The posttherapy tissue usually shows necrosis, fibrosis, mixed inflammatory infiltrates, and xanthogranulomatous inflammation. Because response to therapy is one of the main prognostic variables, the percentage of viable nonteratomatous GCT should be reported, a finding present in up to 50% of resection specimens, even after normalization of serum markers.53 Less than 10% viable tumor cells is a good prognostic factor as defined by the International Germ Cell Consensus Classification Group (IGCCCG).54 Residual viable tumor may be relatively focal; therefore, areas of scarring, necrosis, or hemorrhage should be carefully examined.F: Margins/Vascular Invasion.—Because completeness of excision is also an important prognostic factor, the excision specimens should be inked and the margin status should be reported. Any adherence of the mass to other structures should be carefully described. If there is a question about adherence, consultation with the surgeon is strongly recommended.Incomplete resection of a neonatal, mature teratoma has been reported to recur in adulthood as adenocarcinoma.55,56 The presence of a non–germ cell malignancy in a SGCT is a poor prognostic feature and requires complete surgical excision and consideration of chemotherapy or radiation therapy.Vascular invasion can involve blood vessels or lymphatics. In suspicious cases, blood vessels can be highlighted with immunoperoxidase staining for factor VIII, CD31, or CD34. This staining will not resolve the problem of differentiating lymphatic versus artifactual space involvement by tumor cells. This type of involvement should be called indeterminate.G: Staging.—Clinical and pathologic staging is very important in the prognosis of EGCTs. Unfortunately, there is not an officially recognized, AJCC/UICC TNM staging protocol for EGCTs. The Children's Oncology Group uses a 4-tiered staging system for all EGCTs.12 Surgeons also carefully define anatomic resections specifically for sacrococcygeal EGCTs. The WHO recommends using a modification of the AJCC TNM staging of soft tissue tumors.57 Moran and Suster28 have also proposed a novel staging system specifically for mediastinal GCTs, based on an outcome study of 322 cases.In the Pediatric Oncology Group/Children's Cancer Group Intergroup study,46 there were 22 children with completely resected, extragonadal, immature teratomas, including 6 (27%) with admixed yolk sac tumor. None of the patients received adjuvant chemotherapy. Three of the 22 children (14%) developed recurrent yolk sac tumors, including 1 child with no admixed yolk sac tumor at diagnosis. Each of these children was treated for their recurrence with surgery and platinum-based chemotherapy (cisplatin, etoposide, and bleomycin). The conclusion of the study was that complete surgical excision is effective treatment for children with immature teratomas, with or without admixed yolk sac tumor. The authors noted that patients with extragonadal tumors are a higher risk group and require very careful follow-up. Although adjuvant chemotherapy could be considered in these patients, it is not recommended because of the toxicity of unnecessary chemotherapy and the success of salvage therapy for those children who do relapse.46A rare finding in extragonadal teratomas of very young children is the occurrence of nodal gliomatosis in regional lymph nodes draining the teratoma.58 The authors have had personal experience with such cases in which the finding had no effect on the patient's clinical course and did not seem to warrant a designation of a “metastasis” upstaging the patient. It is thought that the phenomenon is similar to peritoneal gliomatosis in ovarian teratomas.59 Studies suggest that gliomatosis peritonei is a metaplastic phenomenon of pluripotent Müllerian stem cells because it appears to be genetically unrelated to the teratoma.60 It is unclear whether the finding in lymph nodes is clonally related to the teratoma.Surgeons categorize sacrococcygeal teratomas into anatomic types I to IV on the basis of posterior growth (externalization) or anterior or presacral extension (internalization).12,17 Increased patient age, sacrococcygeal location, and grade 2 to 3 immaturity are more frequently associated with an associated admixed yolk sac tumor.7 In addition, the frequency of admixed malignant elements (yolk sac tumor) was found to correlate with the degree of externalized versus internal presacral extension. The association with malignant nonteratomatous elements increases with presacral extension and less externalization.12,17 It is unclear whether this correlation between site and the presence of admixed malignant elements (yolk sac tumor) is truly a function of the local anatomic environment, or if it is related to the age of the patient at presentation. Externalized tumors will present earlier because they are clinically visible.The overall clinical outcome for primary, mediastinal, immature teratoma and nonteratomatous GCTs is reportedly worse than gonadal GCTs, but outcomes are improving with preoperative cisplatin-based combination chemotherapy strategies.61–64 With neoadjuvant chemotherapy, good prognostic factors include completeness of resection, less than 10% viable tumor cells, and low-risk grouping as defined by the IGCCCG's Moran and Suster Proposed Clinical Staging System for Mediastinal GCTs.54In the IGCCCG groupings, there are prognostic differences among histologic subtypes of GCT. Pure mediastinal seminoma has a better outcome than tumors with a nonseminomatous component. The reported 5-year survival of 90% with cisplatin-based combination chemotherapy rivals the outcome of testicular seminomas.61,62,65 Poor prognostic features of pure seminoma include liver or other nonpulmonary visceral metastases and metastases to 2 or more sites.61 Primary mediastinal choriocarcinoma is rare but reportedly has a much worse prognosis than other histologic subtypes owing to the hematogenous dissemination at the time of diagnosis.66 At least some studies that include choriocarcinomas suggest an improved prognosis under current chemotherapeutic regimens.67 Embryonal carcinoma and yolk sac tumor, whether pure or in association with any other components (seminoma or teratoma), have a similar outcome and are generally regarded as poor prognostic findings. As discussed above, mature teratoma is benign, but immature teratoma has some potential for malignant behavior. In stage I pure immature teratomas (ie, no infiltration of adjacent structures and no mixed germ cell elements or secondary malignancy), the risk for aggressive behavior may be fairly low, but clinical outcome data are limited.H: Cytogenetics.—It is well documented that pediatric GCTs are distinct from adult GCTs cytogenetically. Although most adult, malignant GCTs have the isochromosome 12p abnormality, this aberration is very rare in children younger than 10 years.68 Although some yolk sac tumors have shown aberrations of the short arm of chromosome 12 by interphase fluorescence in situ hybridization,69,70 no cytogenetic abnormality has been found to specifically correlate with histology or primary tumor site in children. Aberrations of 1p, 1q, 6q, chromosome and the sex chromosomes are also frequently encountered.68,71 In a Children's Oncology Group study8 of 81 pediatric GCTs (gonadal and extragonadal), the 12p isochromosome was only found in adolescent boys. It remains to be investigated whether isochromosome 12p might be a better prognostic factor than age in the peripubertal period.There is an unusual association between mediastinal GCTs, hematologic malignancies, and cytogenetics.72–79 Although it is unknown why they are associated with only mediastinal tumors, genetic studies have demonstrated that both the GCT and hematopoietic components are clonally related.72,75 The germ cell component is typically a yolk sac tumor, but immature teratomas and other nonseminomatous GCTs are also described. The most commonly associated hematopoietic malignancy is acute myeloid leukemia of megakaryocytic or monocytic differentiation (ie, M7, M4, and M5), which comprises approximately one-half of all cases.65,80,81 Other reported malignancies include the spectrum of acute myeloid leukemia subtypes,79,80 acute undifferentiated leukemia,80 myelodysplastic syndrome,82,83 myeloproliferative disorder,80,84,85 “malignant histiocytosis,” 75 mastocytosis,86 and acute lymphoblastic leukemia.76,80 These hematopoietic tumors may involve the mediastinal GCT or be completely extramediastinal.81 The hematopoietic component frequently shows an isochromosome 12 [i(12p)],72 the most common genetic alteration in GCTs, but may additionally harbor translocations more typical of the specific morphologic phenotype [eg, del(5q), trisomy 8]. This finding suggests that the non-i(12p) aberration determines the tumor phenotype.Germ cell tumor–associated acute leukemias are an ominous finding because they are typically refractory to current treatment modalities, with a reported survival of less than 2 years in all reported patients. The main differential diagnostic consideration in this setting is a therapy-related myelodysplastic syndrome or acute leukemia following etoposide administration.74 Therapy-related diseases can be distinguished by their occurrence later in the course (25 to 60 months), the absence of i(12p), and the possible presence of an etoposide-related translocation, such as 11q23.87–89I: Tissue and Serologic Markers.—Tissue Immunohistochemistry.—Extragonadal GCTs typically show immunoreactivity patterns identical to their gonadal counterparts.90 In general, embryonal carcinoma, yolk sac tumor, choriocarcinoma, and the epithelial elements of teratoma all show cytokeratin AE1/AE3 reactivity. Although cytokeratin AE1/AE3 expression in testicular seminomas has been proposed as a potential marker of early carcinomatous progression,91 this concept has not been addressed in extragonadal sites. A dotlike paranuclear reactivity pattern to low–molecular-weight cytokeratin (ie, CAM 5.2) is seen in up to 80% of mediastinal seminomas.90,92Although placental-like alkaline phosphatase has traditionally been the marker of choice to objectively verify germ cell origin (mostly seminoma) in the setting of an “undifferentiated” neoplasm,93–95 its lack of sensitivity, generally high background staining, and the development of newer antibodies have rendered placental-like alkaline phosphatase less useful in current diagnostic practice. Strong membranous CD117 (c-kit) immunoreactivity has been reported in 75% to 100% of seminomas,94 but it is not specific because it marks other non–germ cell carcinomas in the differential diagnosis, such as lung96 and thymic carcinomas.96–98 In addition, embryonal carcinoma, yolk sac tumor, and choriocarcinoma may show some degree of weak CD117 reactivity. CD30 is also used in the workup of a poorly differentiated malignant neoplasm because it is positive in more than 80% of embryonal carcinomas, but careful morphologic and clinical correlation is required because it also marks a spectrum of hematopoietic malignancies in the differential diagnosis as well.99Newer markers show better specificity for germ cells tumors. Nearly 100% of seminomas and embryonal carcinomas show nuclear reactivity for OCT4, and the specificity within this morphologic differential seems better than other available markers.100–102 OCT4 is rapidly becoming the marker of choice for documenting germ cell origin (ie, seminoma or embryonal carcinoma) in the workup of an undifferentiated neoplasm. Yolk sac tumors and choriocarcinoma show cytoplasmic and membranous reactivity for the oncofetal protein glypican-3, with no significant reactivity in embryonal carcinoma or germinoma.103,104 Most recently, SALL4 has been shown to demonstrate strong nuclear staining in germinoma, embryonal carcinoma, and yolk sac tumors. SALL4 appears more sensitive than either glypican-3 or AFP for the diagnosis of a yolk sac tumor.105,106 The mononuclear trophoblast cells of choriocarcinoma are also reactive for SALL4.Serum AFP is not a reliable marker for yolk sac tumor because of its low sensitivity.107 Serum evaluation of AFP and HCG is frequently more useful than immunohistochemistry.The presence of minute, occult, yolk sac tumor elements in large sacrococcygeal teratomas can be overlooked. Hawkins et al24 described 6 children with mature or immature sacrococcygeal teratomas initially diagnosed in the newborn period, who had the appropriate operation and subsequently had yolk sac tumor recurrences 7 to 33 months later. Histologic detection of foci of yolk sac tumor in sacrococcygeal teratomas is very important because serum AFP levels are not always helpful as a marker, being normally high in the newborn period as a result of fetal production.24 Moreover, primitive gut and liver tissues in preterm teratomas react also with the AFP antibody, which makes establishing the histologic diagnosis of this sometimes subtle malignancy difficult.Most of the tumor recurrences after congenital teratoma are yolk sac tumor, and AFP is useful in following these patients. Neonatal levels are normally elevated, and the initial AFP level does not seem to correlate with the presence or absence of a yolk sac tumor in neonatal teratomas. Postoperative monitoring can be useful because the AFP level should fall after tumor excision, as it normally would in the neonate.7,17Serum β-HCG immunohistochemistry can be used to identify choriocarcinoma. Isolated syncytial trophoblasts can stain positively in seminomas. Evaluation of serum β-HCG is also helpful in establishing the presence of occult choriocarcinoma.J: Associated Syndromes and Malignancies.—Some constitutional syndromes are thought to have an increased incidence of EGCTs, including Klinefelter68,108–113 and Down syndrome.68,114,115 The association of hematopoietic malignancies with mediastinal EGCTs was described in note H (Cytogenetics). Sarcomatous differentiation, which is most frequent in the mediastinum, may occur in association with teratomas or, less commonly, with other malignant GCTs.82,116–120 As in the gonads, secondary squamous cell carcinoma, adenosquamous carcinoma, and colonic-type adenocarcinoma may rarely complicate extragonadal teratomas.120 The presence of sarcomatous or carcinomatous elements portends a very poor prognosis.
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