
Adrenal lymphangioma masquerading as a pancreatic tail cyst
Author(s) -
Hae Il Jung,
Tae Sung Ahn,
Myoung Won Son,
Zisun Kim,
Sang Ho Bae,
Moon Soo Lee,
Chang Ho Kim,
Hyon Doek Cho
Publication year - 2014
Publication title -
world journal of gastroenterology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.427
H-Index - 155
eISSN - 2219-2840
pISSN - 1007-9327
DOI - 10.3748/wjg.v20.i36.13195
Subject(s) - lymphangioma , medicine , pancreas , cyst , adrenal gland , abdomen , epigastric pain , pathology , radiology , surgery , vomiting
Cystic lymphangiomas of the adrenal gland are rare. A 79-year-old female presented in the emergency room with epigastric discomfort, and an immovable mass was palpated in her abdomen upon physical examination. Imaging studies revealed a large cystic lesion in the pancreatic tail. The radiologic impression ruled out the possibility of a mucinous cystic neoplasm, or a pseudocyst in the pancreas. The operative findings demonstrated that the cystic mass originated in the left adrenal gland. A laparoscopic excision of the cystic mass was performed, and immunohistochemistry confirmed that this mass was a lymphangioma of the adrenal gland. Several prior reports have suggested that lymphangioma can mimic renal or splenic cysts. However, lymphangioma cases mimicking pancreatic cysts are very rare.