7 citations
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May 1996 in “PubMed” This article outlines the clinical and histological features of milia grouped in plaques on a 59-year-old woman's face but reports no new research findings.
August 2018 in “Australasian journal of dermatology” This article is a letter discussing a case of cutaneous lymphoid hyperplasia following hyaluronic acid filler injection and fat grafting, reporting no new results.
2 citations
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February 2023 in “Anais Brasileiros de Dermatologia” In this study, pilomatricoma, a benign skin tumor from hair follicle matrix cells, is highlighted as an important consideration when diagnosing painless, firm subcutaneous nodules, with accurate diagnosis relying on histopathological examination.
January 2003 in “Linchuang pifuke zazhi” This case report describes a trichoblastoma in a 58-year-old man's leg, which was successfully excised without recurrence observed after 9 months.
1 citations
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October 2023 in “European Journal of Dermatology” In this study, combining hair transplantation with platelet-rich plasma was found to be more effective than hair transplantation alone in reducing hair loss, improving hair regeneration, and decreasing skin lesions in patients with androgenic alopecia.
1 citations
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May 2025 in “Frontiers in Veterinary Science” This study suggests that recombinant Lumpy Skin Disease Virus strains pose a severe threat to yaks in the Qinghai-Tibet Plateau, causing high mortality and emphasizing the need for targeted control strategies.
September 2011 in “Archives of dermatology” The child was diagnosed with cutaneous leishmaniasis.
37 citations
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March 1998 in “Lupus” This case report describes a patient with SLE and APLS who developed basaloid follicular hamartomas, which persisted despite aggressive treatment for SLE, although hair regrowth occurred.
27 citations
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June 2020 in “Genes” This study identified multiple loss of function variants in the HR gene linked to the unique hair coat phenotype in lykoi cats, also known as werewolf cats.
3 citations
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February 2025 in “Journal of Investigative Dermatology” Lipocartilage is a new type of tissue that affects hair growth and cartilage regeneration.
June 2022 in “Authorea (Authorea)” This case report describes a 59-year-old Afro-American woman diagnosed with lipedematous alopecia, a rare scalp condition of unknown cause.
October 1991 in “Archives of Dermatology” This case report describes a 59-year-old woman with cicatricial alopecia and multiple skin lesions, including nodules and plaques, with biopsy results showing a lymphocytic infiltrate and collagen replacement.
3 citations
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May 2024 in “Skin Appendage Disorders” This study observed that trichoscopy of long-lasting lesions in a chronic stage revealed specific features such as absence of follicular openings, cicatricial patches, and thick arborizing vessels.
April 2020 in “Journal of the Endocrine Society” This case report details a post-menopausal woman with hirsutism and virilization due to rare Leydig cell tumors in both ovaries, underscoring the challenge of detecting such tumors with standard imaging.
23 citations
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February 2003 in “British Journal of Dermatology” This case study describes a 40-year-old man diagnosed with pilotropic mycosis fungoides, a form of folliculotropic cutaneous T-cell lymphoma, characterized by lymphocytic infiltration of hair follicles and eccrine glands.
January 1962 in “Archives of Dermatology” This case report describes a 5-year-old girl with lipoid proteinosis, characterized by a raspy voice, thinning scalp hair, and recurrent crusted lesions leading to pock-like scars.
1 citations
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October 2012 in “QJM” This case report describes a 47-year-old man with a persistent erythematous scaly plaque on his left lower eyelid, unresponsive to conservative treatment, later diagnosed through biopsy.
1 citations
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April 2016 in “British Journal of Dermatology” Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.
November 2022 in “Journal of the Endocrine Society” This case report highlights a rare ovarian steroid cell tumor as the cause of androgen excess in a 36-year-old woman and underscores the importance of thorough preoperative workup to avoid unnecessary surgery.
January 2020 in “Advanced ultrasound in diagnosis and therapy” This case report highlights a misdiagnosis of an epidermoid cyst as a dermoid cyst using ultrasound, suggesting that specific ultrasound features can improve diagnostic accuracy for skin lesions.
1 citations
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January 2013 in “Journal of the Scientific Society” In this case report, an 18-year-old male's cheek lump initially diagnosed as a sebaceous cyst was found to be a pilomatrixoma after surgical excision and histopathological examination.
6 citations
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January 2015 in “Indian Dermatology Online Journal” This case report describes a unique presentation of porokeratotic eccrine ostial and dermal duct nevus with lesions on the dorsum of the hand and a focal lichenoid infiltrate, differing from typical palm and sole involvement.
14 citations
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January 2020 in “Korean Journal of Family Medicine” This case study reported a rare occurrence of lepromatous leprosy with Lucio phenomenon in a 50-year-old Indonesian living in Malaysia, highlighting the necessity for primary care practitioners, even in non-endemic areas, to recognize this serious leprosy reaction to prevent complications and transmission.
9 citations
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May 1989 in “Journal of the Royal Society of Medicine” An elderly woman's swollen, painful foot was found to be caused by a rare type of bone lymphoma, which improved with radiation treatment.
4 citations
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May 2009 in “Clinical and experimental dermatology” This article discusses flexural follicular lichen planus and reports no new clinical findings.
5 citations
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February 2005 in “Journal of the American Academy of Dermatology” Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.
11 citations
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December 2010 in “Archives of Dermatology” This abstract provides no research results, focusing instead on navigation and subscription details for JAMA Dermatology content access.
September 2024 in “Journal of the American Academy of Dermatology” In this case report, a 53-year-old woman with Little-Graham-Piccardi-Lassueur-Syndrome responded well to a treatment regimen of hydroxychloroquine, methotrexate, and other therapies, effectively halting the progression of this rare dermatosis characterized by alopecia and hyperkeratotic eruptions.
9 citations
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August 2002 in “British journal of ophthalmology” This case report describes a young man diagnosed with encephalocraniocutaneous lipomatosis who had unique bilateral optic disc colobomas, a previously unreported association with this syndrome.