An 11-year-old girl with low-grade fever, night sweats, thrombocytopenia, and an 8-year history of progressive splenomegaly underwent an elective splenectomy. Pathologic diagnosis was multiple splenic hamartoma. The patient’s symptoms resolved after the splenectomy. Since first described by Rokitansky in 1861, ;140 cases of splenic hamartoma have been described in the literature. Most of the sp...

An 11-year-old girl with low-grade fever, night sweats, thrombocytopenia, and an 8-year history of progressive splenomegaly underwent an elective splenectomy. Pathologic diagnosis was multiple splenic hamartoma. The patient’s symptoms resolved after the splenectomy. Since first described by Rokitansky in 1861, ;140 cases of splenic hamartoma have been described in the literature. Most of the sp...

An 11-year-old girl with low-grade fever, night sweats, thrombocytopenia, and an 8-year history of progressive splenomegaly underwent an elective splenectomy. Pathologic diagnosis was multiple splenic hamartoma. The patient’s symptoms resolved after the splenectomy. Since first described by Rokitansky in 1861, ;140 cases of splenic hamartoma have been described in the literature. Most of the sp...

Precocious puberty is a rare condition characterized by the development of secondary sexual characteristics before the median age for the sex. It is either gonadotropin dependent also called as central or gonadotropin independent also known as peripheral type. Hypothalamamic Hamartoma is a common cause of the central or precocious puberty due to organic brain lesion. Here we present a two year ...

Hypothalamic hamartoma is a developmental malformation in the region of tuber cinereum and mamillary bodies. It presents the most commonly detectable lesion in patients with precocious puberty and is associated with gelastic seizures. As well as, it can be completely silent to be found only incidentally. Computed tomography (CT) and magnetic rezonans (MR) imaging are preferred imaging modalitie...

entity and is usually associated with polyposis syndromes such as familial polyposis coli, Cowden syndrome, Peutz Jegher syndrome, and Cronkhite-Canada syndrome (1, 2). A few reports have described a gastric hamartoma without polyposis coli (3-5). It is often overlooked due to its clinical insignificance and small size. We report a case of an unusually large sized, fat-containing gastric hamart...

An esophageal hamartoma is a rare, benign germ-cell condition. Most hamartomas are intraluminal tumors located in the upper third of the esophagus. We herein report an unusual case of a pedunculated hamartoma that involved the lower third of the esophagus that was diagnosed incidentally during investigations for epigastric pain. The features noted on endoscopy, endoscopic ultrasound/Doppler end...

Brunner's gland hamartoma is an extremely uncommon benign tumor of the duodenum. Most of the lesions are small, asymptomatic and are detected incidentally. It may rarely attain a large size and produces a variety of clinical manifestations. Imaging modalities and endoscopy may locate the lesion, but definitive diagnosis requires histopathological examination. We report a case of a 58-year-old O...

Lipofibromatous hamartoma is a rare tumor-like overgrowth of fibroadipose tissue surrounding the nerves. Most commonly, it involves the median nerve. The tumor is usually present at birth and grows very slowly. The expected age of clinical presentation is the third or fourth decades of life. The case reported here had a rapid overgrowth and presented at the age of eight. Our case is the first r...