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This source reports that a study by Liu et al. analyzed genetic factors influencing adalimumab response in hidradenitis suppurativa, finding a specific genetic variant (SNP rs59532114) associated with an inadequate response to the treatment due to increased abscess and inflammatory nodule counts.

This case study describes an unusual instance of separate trichoadenoma and melanocytic naevi occurring simultaneously on the face, with the cause of their association remaining uncertain.

In this study, outbreaks of tinea capitis caused by Trichophyton tonsurans were linked to hairdressing in Sardinian barbershops, with 10 young adult men developing the infection following haircuts; timely treatment is crucial to prevent complications like scarring alopecia.

This case study reports on a rare occurrence of trichoadenoma in the vulva of a 25-year-old female, describing typical histological features of the tumor.

This case report describes a unique lesion in a 10-month-old girl, characterized by increased eccrine glands and hair follicles, leading to the proposed term "hybrid eccrine gland and hair follicle hamartoma".

This case report documented a novel presentation of a canine viral plaque appearing as a solitary exophytic keratin-filled mass, highlighting the need to differentiate it from a hair follicle tumor.

This report highlights two cases where trichoblastoma in the breast was initially misdiagnosed as malignancy due to diagnostic challenges in needle core biopsies, emphasizing the importance of expert dermatopathologic review.

Tufted folliculitis is common in patients with folliculitis decalvans.

This study observed that acanthosis nigricans is highly prevalent in Latin American youths, especially at the knuckles, and may indicate early insulin resistance even in those with a normal BMI.

This case study reports a rare occurrence of a large trichobezoar in a 3-year-old male, who presented with a thread protruding from his mouth without any signs of hair loss.

This case report describes the successful surgical removal of a trichobezoar in an 8-year-old girl, which extended from her stomach into the duodenum.

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.

This case report describes a 27-year-old man with a unique association of keratosis follicularis spinulosa decalvans and acne keloidalis nuchae, successfully treated with oral isotretinoin.

This case report describes a 45-year-old man with androgenetic alopecia who developed painful abscesses after monacrylic hair fiber implantation, requiring surgical intervention with tissue expansion and flap repair.

This article discusses the inflammation process in dissecting cellulitis and folliculitis keloidalis, noting the role of follicular rupture and hair fragments while reporting no new results; the authors highlight differences in bacterial presence and pathogenesis understanding.

This case report describes a pilomatricoma in a 21-year-old woman, highlighting the diagnostic process and illustrating the potential for intraoral surgical access to minimize scarring.

This case series examined five male burn patients who developed folliculitis barbae or pseudofolliculitis barbae, highlighting the underreported nature of these complications and the variability in treatment response. The authors call for standardized diagnostic criteria and treatment protocols for these conditions in burn survivors.

In this case report, an 8-year-old boy's crusted scalp lesions and alopecia initially mimicking kerion were ultimately diagnosed as Pre-B acute lymphocytic leukemia after histopathological evaluation revealed leukemia cutis.

Recurrent furunculosis can be managed with antibiotics, decolonization, and decontamination, with potential future use of vaccines and bacteriophage therapy.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

This report describes two cases of nevus lipomatosus superficialis with the unusual feature of dilated hair follicles, emphasizing the need for precise histopathological diagnosis to differentiate from similar conditions.

This case report describes a patient with Clouston Syndrome who developed eccrine syringofibroadenoma, marking only the fourth such association documented in existing literature.

This case report describes a 10-year-old patient with a rare trichilemmal cyst in the cervical region, highlighting the importance of close monitoring due to potential risks of malignancy.

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.

In this case report, the authors observed that understanding the cytological features of trichilemmal carcinoma is crucial for accurate FNAC diagnosis of its metastases in head and neck regions.

This chapter reviews bacterial skin diseases in camelids, such as folliculitis, furunculosis, and others, providing diagnostic insights without presenting new clinical results.

In this case report, researchers identified Arthroderma vanbreuseghemii as the cause of a familial fungal infection, which was successfully treated with itraconazole and topical terbinafine cream.

This case report describes the occurrence of eruptive vellus hair cysts in twin patients, adding to the literature on this dermatological condition.

This study described specific skin and hair follicle abnormalities in three Japanese patients with Cantu syndrome, which may relate to the regulation role of SUR2 in hair follicle growth.