منابع مشابه
Darier-Roussy Sarcoidosis Mimicking Metastatic Breast Cancer
Subcutaneous sarcoidosis (also known as 'Darier-Roussy sarcoid') is a cutaneous condition characterized by numerous deep-seated nodules on the trunk and extremities. Coexistence of sarcoidosis and breast cancer are reported in the literature, but there will always be a chance of misdiagnosis. It is very crucial to obtain a tissue diagnosis of suspicious metastatic lesions. We report a case of b...
متن کاملAcral Hemorrhagic Darier Disease.
Darier disease is an autosomal-dominant inherited condition caused by mutation of a gene, which produces a protein involved in calcium channel regulation. The disease has a variety of manifestations and lacks consistent genotype-phenotype correlations. Acral hemorrhagic Darier disease causes macules, papules, vesicles and/or hemorrhagic blisters on the extremities. Other classic signs of the di...
متن کامل"Residual bodies" in sarcoid and sarcoid-like granulomas.
A MORPHOLOGICAL AND HISTOCHEMICAL STUDY WAS MADE OF EPITHELIOID CELL GRANULOMAS: (a) classical sarcoid type, namely, sarcoidosis, Kveim tests, tuberculosis, farmer's lung, and Crohn's syndrome; (b) sarcoid-like granulomas, often distinguishable from (a) by the presence of extracellular mucin or bile, namely, ulcerative colitis, diverticulitis, cholecystitis, cholangitis, carcinoma of the rectum...
متن کاملDarier disease: a case report.
The diagnosis of Darier disease of the oral mucosa was made only after biopsying a leukoplakia-like lesion of the palate.
متن کامل[Boeck's sarcoid].
The various theories regarding the etiology only serve to demonstrate how much there is yet to be proved about this disease. Boeck originally considered the disease to be a constitutional one, caused by a non-virulent form of tubercle bacillus. This opinion is still held by a large number of men. A comparatively high proportion of cases will later develop an active tuberculosis. Pinner believes...
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1936
ISSN: 0035-9157
DOI: 10.1177/003591573602900707