Adrenal ganglioneuroma in a patient with polycystic ovarian disease (PCOD): a rare association
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چکیده
منابع مشابه
A Novel PKD1 Mutation in a Patient with Autosomal Dominant Polycystic Kidney Disease
متن کاملInflammatory myopathies in a patient with Darier\'s disease, a possible association
Background: Darier disease (DD) is an autosomal dominant genetic disorder which develops from a mutation in the ATP2A2 gene. Inflammatory myopathies (IM) are the largest group of potentially treatable myopathies. In this case, we report development of IM in a patient with DD for the second time in the literature. Case presentation: The patient is a 59-year-old female, a known case of DD,...
متن کاملGanglioneuroma of the Adrenal Gland: A Rare Tumor in a Rare Location
A 62-year-old man presented to his general practitioner complaining of non-specific back pain. He underwent a computerized tomography scan and magnetic resonance imaging that revealed a large left adrenal mass. A thorough investigation of this mass revealed it to be a non-secreting tumor. At surgery, a large tumor of the left adrenal was found. The final pathology report revealed a ganglioneuro...
متن کاملAdrenal ganglioneuroma: a diagnostic challenge.
Ganglioneuroma is a benign neoplasm derived from the neural crest that is mainly located in the mediastinal and peritoneal sympathetic ganglia and, very occasionally, in the adrenal gland. It usually occurs in children or adolescents, causes no or highly nonspecific symptoms, and is typically a non-secreting tumor. Among the neuroblastic tumors, ganglioneuroma is the most uncommon, the one with...
متن کاملIdentification of a Novel Intragenic Deletion of the PHKD1 Gene in a Patient with Autosomal Recessive Polycystic Kidney Disease
Background Autosomal recessive polycystic kidney disease (ARPKD) is caused by mutations in the PKHD1gene. In the present study, we describe a severe case of ARPKD carrying a point mutation and a novel four-exon deletion of PKHD1 gene. Materials and Methods The PKHD1, PKD1 and PKD2 ...
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ژورنال
عنوان ژورنال: Case Reports
سال: 2013
ISSN: 1757-790X
DOI: 10.1136/bcr-2013-201211