Prostatic malakoplakia: a case report with review of the literature
نویسندگان
چکیده
منابع مشابه
MALAKOPLAKIA OF THE COLON: A CASE REPORT AND LITERATURE REVIEW
Malakoplakia is a rare disease with undefined etiology that has been almost exclusively reported in urology and pathology journals. We are presenting a case of colonic malakoplakia in an I8-year old young man who was referred to us with a four-year history of intermittent rectorrhagia. The pathological examination of the endoscopically resected specimen revealed pathognomonic features of ma...
متن کاملRenal transplant malakoplakia: case report and review of the literature
Malakoplakia is a rare inflammatory disorder that affects predominantly the urinary tract and kidneys. Isolated renal parenchymal involvement occurs in 16% of all cases [1]. Urinary tract and digestive malakoplakia have been reported in transplant recipients but involvement in transplant tissue is rare. We report a case of renal allograft parenchymal malakoplakia and present a brief review of k...
متن کاملmalakoplakia of the colon: a case report and literature review
malakoplakia is a rare disease with undefined etiology that has been almost exclusively reported in urology and pathology journals. we are presenting a case of colonic malakoplakia in an i8-year old young man who was referred to us with a four-year history of intermittent rectorrhagia. the pathological examination of the endoscopically resected specimen revealed pathognomonic features of malako...
متن کاملDentigerous Cyst Associated with a Deciduous Tooth: Report of a Case and Review of the Literature
Introdouction: Dentigerous cyst is a benign developmental lesion of the jaw. It is most commonly occurs during the second and third decades of life and has rarely been reported in association with a deciduous tooth. We report a case of two-year old girl who presented with an unerupted central incisor. According to the radiographic findings, she was diagnosed with a dentigerous cyst and...
متن کاملMALIGNANT HISTIOCYTOSIS: A CASE REPORT AND REVIEW OF THE LITERATURE
Malignant histiocytosis (MH) is a rare hematologic malignancy, especially in the first decade of life. The disease is clinically characterized by fever, hepatosplenomegaly, lymphadenopathy, pancytopenia and jaundice, and histologically by systemic proliferation of malignant histiocytes and hemophagocytosis. The prognosis is poor and often the diagnosis is not made before death. Because of ...
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: Journal of Surgical Case Reports
سال: 2018
ISSN: 2042-8812
DOI: 10.1093/jscr/rjy050