Cytological diagnosis of syringocystadenoma papilliferum a rare adnexal tumor
نویسندگان
چکیده
منابع مشابه
Syringocystadenoma Papilliferum of the Bony External Auditory Canal: A Rare Tumor in a Rare Location
Tumors originating from ceruminous glands are rare lesions of the external auditory canal. The lack of specific clinical and radiological signs makes their diagnosis challenging. We report the case of an exceptionally rare benign tumor, a syringocystadenoma papilliferum (SCAP), in an atypical location in the bony segment of the external auditory canal with uncommon clinical signs. The special t...
متن کاملGiant naevoid syringocystadenoma papilliferum.
Sir, Syringocystadenoma papilliferum (SCAP) is a rare tumour first described in 1893 (1). To date, 400 cases have been reported worldwide. SCAP usually appears at birth or in early childhood, most frequently on the face or scalp. In approximately 25% of cases it is observed on other locations such as the trunk or the extremities. In 40% of cases, SCAP evolves contiguous to a pre-existing naevus...
متن کاملGiant linear syringocystadenoma papilliferum on scalp.
minutes 00 seconds), clotting time (4 minutes 10 seconds), active partial thrombin time (27.4 seconds; normal range-24-32 seconds), prothrombin time, blood peripheral smear examination, liver function tests and renal function tests were all within normal limits. Urine and stool examination did not reveal erythrocytes or any abnormalities. Upper gastro-intestinal endoscopy and ultrasound of the ...
متن کاملGiant condyloma acuminata with syringocystadenoma papilliferum.
350 six months. The same lesion had gradually increased to attain the present size. Family and personal history were not contributory. Dermatological examination revealed two skin lesions on the medial aspect of the right thigh [Figure 1]. The larger one was 6 × 7 cm in size and smaller one was 1 × 3 cm in size. Both were firm in consistency, non-tender, mobile on the underlying structure, caul...
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ژورنال
عنوان ژورنال: Journal of Cytology
سال: 2015
ISSN: 0970-9371
DOI: 10.4103/0970-9371.160571