Results 51 to 60 of about 1,367 (175)
Anais Brasileiros de Dermatologia, 2014 Incontinentia pigmenti is a rare genodermatosis in which the skin involvement occurs in all patients. Additionally, other ectodermal tissues may be affected, such as the central nervous system, eyes, hair, nails and teeth.
Claudia Schermann Poziomczyk +12 more
doaj +1 more source
The Journal of Dermatology, Volume 52, Issue 12, Page 1763-1774, December 2025.ABSTRACT No consensus was made on whether all Nevus sebaceous (NS) should undergo prophylactic excision and the best age of surgery. This is a retrospective study. Patients who underwent surgery and were confirmed as NS by pathology during January 2014 to December 2023 in the Department of Dermatology of Xinhua hospital were included in this study.
Wange Zhou +5 more
wiley +1 more source
Chronic cutaneous lupus erythematosus in a blaschkoid pattern over face
Indian Journal of Dermatology, 2018 Linear lesions following the lines of Blaschko of chronic cutaneous lupus erythematosus is a highly unusual variant of cutaneous lupus, particularly in adult.
Manju Meena +3 more
doaj +1 more source
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT Williams syndrome (WS) is a rare congenital multi‐systemic condition due to gene deletion. We present a rare case of co‐existence of WS, port wine stains, and phacomatosis pigmentovascularis. This case emphasizes the importance of recognizing the co‐occurrence of such conditions and WS for accurate diagnosis and management.
Bahareh Abtahi‐Naeini +2 more
wiley +1 more source
Focal dermal hypoplasia: A rare case report
Indian Journal of Dermatology, 2015 Focal dermal hypoplasia (Goltz syndrome) is a rare genetic multisystem disorder primarily involving the skin, skeletal system, eyes, and face. We report the case of an eight-month-old female child who presented with multiple hypopigmented atrophic ...
Sahana M Srinivas, Ravi Hiremagalore
doaj +1 more source
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT Partial unilateral lentiginosis (PUL) is a rare pigmentary disorder characterized by numerous lentigines grouped within normal skin in a segmental pattern with sharp demarcation at the midline. The authors hereby present a case of a 40‐year‐old female, who presented with multiple asymptomatic, gradually progressive, brownish flat skin lesions ...
Niranjan Pudasaini +5 more
wiley +1 more source
Blaschkoid Facial Lesion in an Adult Woman
JEADV Clinical Practice, Volume 5, Issue 1, Page 340-342, March 2026.
João Teixeira +4 more
wiley +1 more source
Extragenital lichen sclerosus et atrophicus along the lines of Blaschko
Indian Dermatology Online Journal, 2015 Lichen sclerosus et atrophicus (LSA) is a chronic inflammatory dermatosis of unknown etiology. Extragenital involvement is uncommon and commonly affects the neck, shoulders, and upper portion of the trunk. It is predominant in women with a male-to-female
Nilofar G Diwan, Pragya A Nair
doaj +1 more source
Sclerosing diseases of the skin
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 10, Page 1282-1301, October 2025.Summary Sclerosing skin diseases comprise a group of distinct dermatological conditions characterized by fibrotic changes that may severely impair patients’ quality of life. These conditions often present with cutaneous manifestations and, in some cases, may extend to extracutaneous tissues, potentially resulting in significant morbidity and mortality.
Yasamin Kalantari +4 more
wiley +1 more source
Progressive cribriform and zosteriform hyperpigmentation
Indian Dermatology Online Journal, 2014 Here we report a case of a healthy 30-year-old male who presented to us with progressively increasing reticulate pigmented lesions following lines of Blaschko on the right side of abdomen and back.
Rameshwar M Gutte
doaj +1 more source