منابع مشابه
A Ruptured Digital Epidermal Inclusion Cyst: A Sinister Presentation
Epidermal inclusion cysts are benign cutaneous lesions caused by dermal or subdermal implantation and proliferation of epidermal squamous epithelium as a result of trauma or surgery. They are typically located on the scalp, face, trunk, neck, or back; however they can be found anywhere on the body. Lesions are asymptomatic unless complicated by rupture, malignant transformation to squamous cell...
متن کاملRuptured Hemorrhagic Cyst of Undescended Ovary Mimicking Mucocele: A Rare Pediatric Case
Undescended ovary is a rare entity and usually presentedas a case report. It is associated with urinary and uterine anomalies. Symptomatic patients are diagnosed during surgery. Most of the patients are asymptomatic and treatment is unnecessary. They are incidentally diagnosed during infertility evaluation and treatment such as ovarian hyperstimulation studies.A 15-year-old female patient prese...
متن کاملMalignant epidermal cyst: a case report.
INTRODUCTlON Although malignancy developing in an epidermal cyst has been described,' the rarity of such an occurrence has been emphasised.2 73 34 A review of the English literature also revealed that metastatic disease in a malignant epidermal cyst has not been described. This paper reports a malignant epidermal cyst with metastatic disease and considers features which may be relevant t o its ...
متن کاملHemobilia caused by a ruptured hepatic cyst: a case report
INTRODUCTION Hemobilia is a rare cause of upper gastrointestinal bleeding. More than 50% of hemobilia cases are related to iatrogenic trauma from hepatobiliary procedures, and needle biopsy of the liver represents the most common cause. A minority of hemobilia cases are due to hepatobiliary disorders such as cholangitis, hepatobiliary cancers, choledocholithiasis, and vascular abnormalities in ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Cureus
سال: 2020
ISSN: 2168-8184
DOI: 10.7759/cureus.11099