Case of Malakoplakia
نویسندگان
چکیده
منابع مشابه
A Case Study of MalakoplakIa Disease
Malakoplakia is a pseudogranulomatous disorder secondary to an still unknown de - feet in some stages of phagocytosis. We have reported a 3 year-old girl afflicted with this defect, who was admitted to Loghman Hospital' Pediatrics Department with severe pallor, abdominal mass and loonstanding history of dysentery prior to hospitalisation. Inconclusive clinical and B.M. Investigations rendered...
متن کاملCASE REPORTS Malakoplakia of colon
Malakoplakia, first described by Michaelis and Gutmann in 1902 [1], occurs mainly in the genitourinary tract (60% of cases), and less frequently in the gastrointestinal tract (10% of cases) [2]. Although the pathogenesis of malakoplakia is not completely understood, the disease may be considered the result of an impairment of the mononuclear phagocyte and immunoregulatory effector system [3]. T...
متن کاملMalakoplakia of the spleen: a case report.
Malakoplakia is an uncommon chronic inflammatory disorder, which is characterized by the presence of histiocytes containing concentric concretions known as Michaelis-Gutmann bodies in a background of mixed inflammation. The urinary tract is the most commonly involved site. However, malakoplakia can be found in a wide range of other organs throughout the body. Its occurrence has been attributed ...
متن کاملMalakoplakia of Proximal Tibia- A Case Report
INTRODUCTION Malakoplakia is chronic granulomatous disorder resulting from an abnormal immunological response resulting in accumulation of histiocytes [1].It normally involves the urinary bladder, colon, skin etc. But bone is rarely involved. Only seven cases have been reported in the literature. Ours is the first case involving the tibia. CASE REPORT We report a rare case of malakoplakia of ...
متن کاملCutaneous malakoplakia: case report and review*
Malakoplakia is a rare acquired disease that can affect many systems but is more common in the urogenital tract. Cutaneous malakoplakia is even rarer. It is far more frequent in immunodeficient patients. We report a case of cutaneous malakoplakia in a kidney transplant patient who had recently stopped receiving immunosuppressive therapy to illustrate a review of the relevant recent literature.
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1923
ISSN: 0035-9157
DOI: 10.1177/003591572301602206