Results 21 to 30 of about 1,372 (183)

Cytopathological findings of proliferating pilomatricoma misdiagnosed as a malignant parotid gland tumor

open access: yesDiagnostic Pathology, 2018
Background Pilomatricoma is a relatively common benign cutaneous adnexal neoplasm with differentiation towards the hair matrix, inner sheath of hair follicle and hair cortex. Proliferating pilomatricoma is a rare variant of pilomatricoma that can rapidly
Nozomu Kurose   +7 more
doaj   +2 more sources

Clinicopathological features of pilomatricoma cases: Analysis of 21 cases [PDF]

open access: yesJournal of Pathology of Nepal, 2014
Background: Pilomatricoma is a slow-growing, asymptomatic tumour originating from outer sheath cells of hair follicle. In this study, we describe the clinical presentation and histopathological features of pilomatricoma.
D Ghartimagar   +5 more
doaj   +2 more sources

Pilomatricoma In A 18 Years Female

open access: yesIndian Journal of Dermatology, 1998
A 18 year girl presented with an asymptomatic solitary nodule on the lateral aspect of the right below. Biopsy proved it to be Pilomatricoma. The lesion was excised.
Banerjee Uttam   +2 more
doaj   +1 more source

Pilomatricoma mimicking ruptured epidermal cyst in a middle aged woman

open access: yesIndian Journal of Dermatology, 2016
Pilomatricoma is a benign tumor arising from the hair matrical cells. Most pilomatricomas appear in the first two decades of life as a solitary skin to a bluish colored nodule on head-neck area with an occasional sign of inflammation.
Sudip Sarkar   +3 more
doaj   +2 more sources

Line-Field Confocal Optical Coherence Tomography (LC-OCT) of Pilomatricoma. [PDF]

open access: yesPediatr Dermatol
ABSTRACT Pilomatricoma is a benign cutaneous tumor of hair matrix origin, often presenting in children as a slow‐growing, firm, colored nodule. Line‐field confocal optical coherence tomography (LC‐OCT) is a novel imaging method that enables non‐invasive, quasi‐histologic visualization of the skin.
Palmisano G   +8 more
europepmc   +2 more sources

Pilomatricoma as a diagnostic pitfall in clinical practice: Report of two cases and review of literature

open access: yesIndian Journal of Dermatology, 2010
Pilomatricoma (PMC) is a relatively uncommon benign skin neoplasm arising from the skin adnexa. Since the first description of PMC in 1880, there has been a gradual increase in understanding of the morphologic features and clinical presentation of this ...
Pant Ishita   +3 more
doaj   +1 more source

Pilomatricoma: epitelioma calcificado de Malherbe Pilomatricoma: calcifying epithelioma of Malherbe

open access: yesRevista Brasileira de Cirurgia Plástica, 2012
INTRODUÇÃO: Pilomatricoma (epitelioma calcificante de Malherbe) representa cerca de 1% dos tumores benignos de pele. O objetivo deste estudo retrospectivo é rever as características clínicas e histopatológicas dessa lesão em pacientes tratados nos ...
Rebeca Paohwa Liu da Fonseca   +6 more
doaj   +1 more source

Clinically ulcerated and granulomatous pilomatricoma in a cutaneous vaccination site: case report [PDF]

open access: yesSurgical & Cosmetic Dermatology, 2022
Pilomatricoma is a benign skin tumor derived from the hair follicle. It has a varied etiology, and the traumatic one is often described as a triggering factor. The surgical treatment is curative and, therefore, the choice.
Rodrigo Scabora   +5 more
doaj   +1 more source

Pilomatricoma With Bullous Appearance: A Case Report

open access: yesInternational Journal of Dermatology and Venerology, 2023
Introduction:. Pilomatricoma is usually a solitary, deep dermal firm nodule with an overlying normal epidermis. Bullous pilomatricoma is rarely reported; thus, its pathogenesis has not been elucidated.
Yue-Ying Fan   +3 more
doaj   +1 more source

No Evidence of Abnormal Expression of Beta-Catenin and Bcl-2 Proteins in Pilomatricoma as One Clinical Feature of Tetrasomy 9p Syndrome

open access: yesInternational Journal of Pediatrics, 2021
Background. Little is currently known about the genetics of pilomatricoma. A number of studies have reported some evidence that this disease may have a genetic association with mutations of CTNNB1 gene or expression of the beta-catenin protein.
Chariyawan Charalsawadi   +6 more
doaj   +1 more source

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