| Literature DB >> 25278717 |
Hae Il Jung1, Taesung Ahn1, Myoung Won Son1, Zisun Kim1, Sang Ho Bae1, Moon Soo Lee1, Chang Ho Kim1, Hyon Doek Cho1.
Abstract
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.Entities:
Keywords: Adrenal gland; Cyst; Lymphangioma; Mucinous neoplasm; Pancreas
Mesh:
Substances:
Year: 2014 PMID: 25278717 PMCID: PMC4177502 DOI: 10.3748/wjg.v20.i36.13195
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742