SYRINGOCYSTADENOMA PAPILLIFERUM OF SCALP – A CASE REPORT OF A RARE CUTANEOUS ADNEXAL NEOPLASM

Author:

Chatragadda Ramya1,Monika Chilakala Venkata2,Nalubola Saketh2

Affiliation:

1. Assistant professor of General Surgery, Osmania General Hospital, Hyderabad

2. Post graduate resident of general surgery, Osmania General Hospital, Hyderabad

Abstract

Syringocystadenoma papilliferum is a rare benign hamartomatous tumor arising from apocrine or eccrine sweat glands with a predilection for head and neck. Here we report a case of a 30 year old female who presented to our opd with a nodule over scalp since birth which turned into a hairless , exophytic pinkish growth with blood tinged discharge slowly over the last 2 years . A punch biopsy of the lesion revealed syringocystadenoma papilliferum. Excision of the lesion is performed and specimen is sent for (hpe) histopathological examination which revealed syringocystadenoma papilliferum with no malignant transformation. Post operative recovery was uneventful and the patient was followed up till 6 months with no history of recurrence.

Publisher

World Wide Journals

Reference9 articles.

1. Stokes JH. A clinico-pathologic study of an unusual cutaneous neoplasm combining nevus syringadenomatosus papilliferus and a granuloma. J Cutan Dis 1917;35:411-9.

2. Atlas and synopsis of Lever’s histopathology of the skin - 3rd edition . Page numbers 363-364.

3. Dermatologic surgery by Allison T Vidimos, Christie T Ammirati , Christine Poblete-Lopez. Chapter 16 page 199-206.

4. Pinkus H. Life history of naevus syringocystadenomatosus papilliferus. Arch Dermatol Syphilol 1954; 69: 305-22.

5. Atlas and synopsis of Lever’s histopathology of the skin - 3rd edition . Page numbers 363-364.

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