This study focal points a rare case order of chondroid syringoma in three young patients. Chondroid syringoma is as known or named at another time or place mixed tumour of the skin. It is an exceptional, biphasic cutaneous neoplasm that features a salivary gland pleomorphic adenoma. Because it is so uncommon, many cases are originally misdiagnosed as cysts or other cutaneous adnexal neoplasms, and are commonly only discovered later being sent for histopathological experiment. The tumour is composed of a conception of epithelial cells present in a myxoid and chondroid forge. Although chondroid syringoma was predominantly mild, sweat-gland tumour, the usual performance is of an asymptomatic, slowly increasing mass, usually located on the head and narrow connector region. Although it regularly presents in middle and older old patients, we are giving three younger inmates with Chondroid syringoma, situated over the back, nose and cheek, individually. It is difficult to pronounce chondroid syringoma clinically or radiologically. All of our cases were misdiagnosed. Excisional biopsy accompanying histopathological examination and histochemical stains debris the gold standard.
Author(s) Details:
Nechal Kaur,
Department of Pathology, Maharishi Markandeshwar
Medical College and Hospital, Solan, Himachal Pradesh, India.
Neelam
Gupta,
Department
of Pathology, Maharishi Markandeshwar Medical College and Hospital, Solan,
Himachal Pradesh, India.
Vikas Dubey,
Department of Pathology, Maharishi Markandeshwar Medical College and
Hospital, Solan, Himachal Pradesh, India.
Neetu Bala,
Department of Pathology, Maharishi Markandeshwar Medical College and
Hospital, Solan, Himachal Pradesh, India.
Please see the link here: https://stm.bookpi.org/NAMMS-V6/article/view/10993
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