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Congenital Giant Folliculosebaceous Cystic Hamartoma of Thigh: A Rare Case.

التفاصيل البيبلوغرافية
العنوان: Congenital Giant Folliculosebaceous Cystic Hamartoma of Thigh: A Rare Case.
المؤلفون: Bobde VM; Department of Pathology, Government Medical College, Nagpur, Maharashtra, India., Helwatkar SB; Department of Pathology, Government Medical College, Nagpur, Maharashtra, India., Sathawane PR; Department of Pathology, Government Medical College, Nagpur, Maharashtra, India., Raut WK; Department of Pathology, Government Medical College, Nagpur, Maharashtra, India.
المصدر: Indian journal of dermatology [Indian J Dermatol] 2019 Nov-Dec; Vol. 64 (6), pp. 490-492.
نوع المنشور: Case Reports
اللغة: English
بيانات الدورية: Publisher: Medknow Publications Country of Publication: India NLM ID: 0370750 Publication Model: Print Cited Medium: Internet ISSN: 1998-3611 (Electronic) Linking ISSN: 00195154 NLM ISO Abbreviation: Indian J Dermatol Subsets: PubMed not MEDLINE
أسماء مطبوعة: Publication: Mumbai : Medknow Publications
Original Publication: Calcutta : Indian Association of Dermatologists, Venerologists and Leprologists, West Bengal Branch.
مستخلص: Hamartomatous conditions of skin are comprised of variable composition of normal skin elements. They can present as nodular masses. They can be mistaken for neoplastic skin lesions. Folliculosebaceous cystic hamartoma is a rare skin condition seen in adults, commonly on head, neck and face region. Congenital variant is rare. Only few case reports have been described in literature occurring on sites other than face. Definitive diagnosis can be given only on histopathology. We report a case presenting as thigh mass in a 1 year old female child clinically diagnosed as papilloma of skin.
Competing Interests: There are no conflicts of interest.
(Copyright: © 2019 Indian Journal of Dermatology.)
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فهرسة مساهمة: Keywords: Congenital; folliculosebaceous cystic hamartoma; papilloma
تواريخ الأحداث: Date Created: 20200104 Latest Revision: 20200108
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC6862363
DOI: 10.4103/ijd.IJD_319_18
PMID: 31896850
قاعدة البيانات: MEDLINE
الوصف
تدمد:1998-3611
DOI:10.4103/ijd.IJD_319_18