Results 31 to 40 of about 3,478 (138)

WNT10A, dermatology and dentistry

open access: yesBritish Journal of Dermatology, Volume 185, Issue 6, Page 1105-1111, December 2021., 2021
Summary WNTs (Wingless‐related integration sites) are secreted glycoproteins that are involved in signalling pathways critical to organ development and tissue regeneration. Of the 19 known WNT ligands, one member of this family, WNT10A, appears to have specific relevance to skin, its appendages and teeth.
B. J. Doolan   +3 more
wiley   +1 more source

Use of Reflectance Confocal Microscopy for Hidrocystomas: An Emerging, Cost‐Effective, and Powerful Tool

open access: yesCase Reports in Dermatological Medicine, Volume 2021, Issue 1, 2021., 2021
Reflectance confocal microscopy (RCM) is an emerging and noninvasive imaging tool in dermatological practice. Benefits of this modality include differentiation between benign and malignant skin lesions, prevention of unnecessary biopsies, and cost effectiveness. However, RCM findings for benign lesions are rarely reported in the literature. We describe
Amanda Walker   +4 more
wiley   +1 more source

Apocrine hidrocystoma of the cheek [PDF]

open access: yes, 2010
BACKGROUND: Apocrine hidrocystoma is an uncommon benign cystic proliferation of the apocrine sweat glands. Malignant melanoma, eccrine hidrocystoma, angioma, and follicular cysts have to be considered as differential diagnoses.
Bredell, MG   +4 more
core   +1 more source

Apocrine adenocarcinoma in the setting of apocrine hidrocystoma of the leg [PDF]

open access: yes, 2019
Apocrine hidrocystoma is a benign, cystic lesion often presenting in the periorbital region. Apocrine adenocarcinoma is the rare, malignant counterpart occurring mainly in the axilla and anogenital region.
Magro, Cynthia M   +5 more
core   +1 more source

A giant apocrine hidrocystoma of the trunk [PDF]

open access: yes, 2017
Hidrocystomas are benign cysts that typically present as translucent, bluish dermal nodules on the face and are rarely > 1 cm in size. They are classically categorized as eccrine or apocrine based on histologic features.
Compton, Nicholas   +2 more
core   +1 more source

Multiple Apocrine Hidrocystomas: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2013
Hidrocystomas are rare cystic lesions that form benign tumours of the sweat glands. In this report, a clinical case of multiple apocrine hidrocystomas on both the upper and lower eyelids, and on both the malar regions has been discussed. These lesions
Vani D   +4 more
doaj   +1 more source

Treatment of Recurrent Primary Cutaneous Mucinous Carcinoma of the Eyelid with Modified Wide Local Excision

open access: yesCase Reports in Ophthalmological Medicine, Volume 2020, Issue 1, 2020., 2020
Primary cutaneous mucinous carcinoma (PCMC) is a rare, low‐grade malignant neoplasm of the sweat gland, whose history has been controversial regarding eccrine versus apocrine origin. This case report describes a 53‐year‐old male who presented to the University of Florida, Gainesville, ophthalmology clinic and was referred to the oculoplastics service ...
Stephanie M. Tillit   +4 more
wiley   +1 more source

Giant pigmented apocrine hidrocystoma of the scalp [PDF]

open access: yes, 2020
Hidrocystomas are benign cysts of sweat duct epithelium that can present as single or multiple lesions, with or without pigmentation. The size is typically 1-3mm in diameter. Although hidrocystomas commonly occur in most parts of the head and neck region,
Huttenbach, Yve T   +5 more
core   +1 more source

Congenital sudoriferous cyst of the orbit: A case report and review of literature

open access: yesJournal of Cleft Lip Palate and Craniofacial Anomalies, 2017
Apocrine gland cyst (sudoriferous cyst and apocrine hidrocystoma) is fairly uncommon in the eyelid, where it derives from the apocrine glands of Moll. In rare instances, an apocrine gland cyst can occur in the anterior portion of the orbit. If an orbital
Parit S Ladani   +3 more
doaj   +1 more source

Schopf–Schulz–Passarge syndrome

open access: yesIndian Dermatology Online Journal, 2018
Schopf–Schulz–Passarge syndrome (SSPS) is a rare type of ectodermal dysplasia that has autosomal recessive inheritance. It is characterized by palmoplantar keratoderma, hypodontia, hypotrichosis, nail dystrophy, and multiple periocular and eyelid ...
Kinjal D Rambhia   +3 more
doaj   +1 more source

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