Axillary Lymphangioma Research Articles

Surgical Management of a Large, Adult-Onset Axillary Lymphangioma

Surgical Management of a Large, Adult-Onset Axillary Lymphangioma

Axillary lymphangioma that developed following COVID-19 vaccination: a case report

BackgroundExtensive vaccination programs are being implemented worldwide for coronavirus disease 2019 (COVID-19). With the spread of vaccination, swelling of the lymph nodes after vaccination is frequently seen. We encountered a patient who developed left axillary lymphadenoma following vaccine administration.Case presentationThe patient was a Japanese woman in her 80 s who had previously undergone surgery for right breast cancer. She received two injections of the Pfizer-BioNTech COVID-19 vaccine in her left arm. Approximately 3 months later, she complained of left axillary swelling, and imaging resulted in a diagnosis of left axillary lymphangioma. In accordance with the patient’s wishes, we performed axillary mass resection. The pathological diagnosis was lymphangioma.ConclusionOur examination findings indicated that congestion of the axillary lymph vessels might have been caused by upper-arm injections of the COVID-19 vaccine.

AXILLARY AND BREAST LYMPHANGIOMA: AN UNUSUAL CAUSE OF BREAST AND AXILLARY LUMP IN ADULT PATIENTS

Lymphangioma is a benign congenital lymphatic tumor of the lymphatic system due to developmental anomalies. Lymphangioma is commonly seen in the infant and pediatric age groups. In this study, we presented a rare case of axillary and breast lymphangioma in an adult female patients. Patient 24 -year-old lady presented with a large swelling around 15 x 10 cm in the breast and axilla since 6 months of duration. Clinical and radiological examinations were suggestive of breast and axillary lymphangioma. Patient underwent complete surgical resection and diagnosis conrmed on histopathological examination. Lymphangioma of the breast and axilla in adulthood is very rare and very few cases have been reported in the literature. Evaluation for breast cystic lymphangioma should be considered for a prompt diagnosis and denitive treatment to prevent recurrence and complications First line of treatment is surgery with safe margins.

EP05.06: Distal Trisomy 10q: a rare genetic abnormality with unusual presentation as fetal axillary lymphangioma

EP05.06: Distal Trisomy 10q: a rare genetic abnormality with unusual presentation as fetal axillary lymphangioma

Local Bleomycin Treatment in a Newborn with Axillary Lymphangioma: A Case Report

Kistik lenfanjiom, genellikle boyun ve aksilla bolgesinde ortaya cikarken, daha az oranda meme dokusu, abdomen, mediasten, orbita, paratiroid ve ekstremitelerde de gorulebilir. Son yillarda lenfanjiom tedavisinde bleomisin ve picibanil (OK-432) sklerozan tedavi uygulamalari ile basarili sonuclar alindigi bildirilmektedir. Bu yazida hastanemizde takipli olmayan gebelik sonucunda dogumda aksiller lenfangiom tanisi konulduktan sonra kitle icine bleomisin tedavisi uygulanan bir olgu sunulmustur.

P12.02: Early prenatal diagnosis of fetal axillary lymphangioma with ipsilateral pes equinovarus

<scp>P</scp>12.02: Early prenatal diagnosis of fetal axillary lymphangioma with ipsilateral pes equinovarus

Cases of atypical lymphangiomas in children.

Background. Lymphatic malformations or lymphangiomas are rare benign hamartomas that result from maldevelopment of primitive lymphatic sacs. They are most frequently found in the neck and axilla, while intra-abdominal and mediastinal lymphangiomas are uncommon. These are primarily tumours of infancy and childhood and are successfully treated with surgical excision. Summary of Cases. Five cases of lymphangioma comprising three intra-abdominal lymphangiomas and two unilateral axillary lymphangiomas presenting at one institution in Trinidad W.I. between 2005 and 2012 were examined. The presentations, location, workup, treatment, and outcome of these patients were studied. Conclusion. This paper discusses a range of extracervical lymphangioma cases seen at San Fernando General Hospital, Trinidad W.I. We report three intra-abdominal cases and the most common clinical presentations were abdominal pain and distension. Also two axillary cases were reported, which presented as painless axillary masses. The major concerns for excision of axillary lymphangioma by parents and surgeons were cosmesis and feasibility of complete resection without disruption of developing breast tissue and axillary vessels. We believe that ultrasound scan is very good at detection of the lesion, while CT is better at determining tumour content and planning for the operation. It is our opinion that complete surgical excision can be achieved.

İyi prognoz gösteren fetal dev aksiller lenfanjioma

İyi prognoz gösteren fetal dev aksiller lenfanjioma

P14.20: Prenatal diagnosis of a large axillary cystic lymphangioma

P14.20: Prenatal diagnosis of a large axillary cystic lymphangioma

P02.82: Functional ultrasonography: choosing the mode of delivery in a patient with large axillary cystic lymphangioma

P02.82: Functional ultrasonography: choosing the mode of delivery in a patient with large axillary cystic lymphangioma

OC166: Imaging and histopathological features of fetal cortical malformations

(7 cleft lip or cleft lip and palate, 2 cyst of oral cavity), chest (3 right diaphragmatic hernia, 1 sequestration, 3 displaced heart, 1 thymic hyperplasia, 1 axillary lymphangioma), urinary system (1 duplex kidney), abdomen (4 bowel dilatation, an intra-hepatic artero-venous fistula, a pelvic cyst, 1 ascites and bowel calcifications), were represented. Results: In 27 of 32 cases with CNS anomalies, US and MR provided diagnostic images of similar and adequate quality. In the 5 remaining cases US performed better. The antenatal diagnosis was however confirmed after birth in all cases. Among the fetuses with extraCNS anomalies, either antenatal MR or postnatal findings were consistent with sonographic diagnosis in 22 out of 26 cases. A discordance between MR and US was noted in 3 cases. In two fetuses with sonographic diagnosis of cleft lip an unsuspected cleft palate was revealed at MR and confirmed after birth. In a fetus with right deviation of the heart and normally placed stomach, intrathoracic bowel loops were detected at MR and diaphragmatic hernia was documented after birth. The antenatal diagnosis was not confirmed after birth in one case of meconium peritonitis, an abdominal teratoma was diagnosed postnatally. Conclusions: In our own experience, ultrasound and MR performed similarly in CNS anomalies, and ultrasound provided in general better results in early gestation. It is of note that MR was superior in the specific diagnosis and surgical staging of cranial clefts.

P168: Prenatal diagnosis of a large axillary cystic lymphangioma by three-dimensional ultrasound and magnetic resonance imaging

P168: Prenatal diagnosis of a large axillary cystic lymphangioma by three-dimensional ultrasound and magnetic resonance imaging

Fetal axillary lymphangioma complicating breech delivery.

A case of massive lymphangioma arising from the axilla and complicating a breech delivery is described. From research of the literature it is believed that this is the only such case recorded.