منابع مشابه
adrenal cystic lymphangioma presented with hypertension: a case report
conclusions in evaluation of adrenal masses cystic lymphangioma should be considered as a differential diagnosis. introduction adrenal cystic lymphangioma is a rare benign tumor, which is nearly always asymptomatic and incidentally discovered during routine imaging work-ups or investigating other pathologies. case report a 43-year-old female presented hypertension, which during routine work-up ...
متن کاملAdrenal Cystic Lymphangioma Presented With Hypertension: A Case Report
INTRODUCTION Adrenal cystic lymphangioma is a rare benign tumor, which is nearly always asymptomatic and incidentally discovered during routine imaging work-ups or investigating other pathologies. CASE REPORT A 43-year-old female presented hypertension, which during routine work-up of her newly diagnosed hypertension an adrenal mass was discovered and after operation the pathologic diagnosis ...
متن کاملCystic pancreatic lymphangioma
Lymphangioma of the pancreas is a rare benign tumor of lymphatic origin. Retroperitoneal lymphangiomas account for 1% of all lymphangiomas. Herein, we report a case of cystic pancreatic lymphangioma diagnosed in 34 year-old female patient who was hospitalized for a slight pain in the epigastrium and vomiting. Radiological imaging revealed a large multiloculated cystic abdominal mass with enhanc...
متن کاملSolitary cystic mediastinal lymphangioma.
Solitary cystic mediastinal lymphangioma (CML) is a very uncommon benign vascular tumour developed from lymphatic vessels. Cystic lymphangioma is a cyst caused by a congenital malformation of the lymphatic vessels and can affect any site in the body, but ,1% of lymphangiomas are mediastinal [1] and pulmonary lesions are even less common. They are most often located in the anterior mediastinum. ...
متن کاملRetroperitoneal cystic lymphangioma.
A case of a large retroperitoneal tumor in a previously asymptomatic twenty-two-year-old white female is presented. A review of the literature confirms the rarity of this tumor. Its histologic and embryologic derivation as well as its subtle and bizarre method of presentation are discussed. The cause of such lesions is debatable, but primary cure can be accomplished by meticulous excision of th...
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ژورنال
عنوان ژورنال: West Indian Medical Journal
سال: 2015
ISSN: 0043-3144
DOI: 10.7727/wimj.2014.116