Search

everythingexperts & clinicslearnfaqsresearchcommunity

for

Search:↓

This study compared trichostasis spinulosa with keratosis pilaris and eruptive vellus hair cysts, finding differences in lesion distribution and microscopic appearance.

This case report describes dermoscopic features of pemphigus vulgaris on the scalp, highlighting that hair casts may suggest treatment adjustment for improved disease control.

Skin problems can indicate different diseases inside the body.

This case report describes a 4-year-old boy with congenital alopecia characterized by complete irreversible hair loss and papular lesions associated with keratin-filled cysts.

In this study, the KPAI and KP-IGA scoring systems for assessing keratosis pilaris showed excellent interrater and intrarater reliability, offering standardized measures for clinical and research use.

This article reviews congenital and developmental skin conditions in foals and reports no new clinical results; it notes that these conditions can be influenced by genetic and environmental factors.

The child was diagnosed with cutaneous leishmaniasis.

This study found that hyperpigmented skin changes resembling Schamberg’s purpura occur in areas affected by CRPS and can also appear on mirror-image locations of unaffected limbs, potentially improving with the condition's treatment.

This article presents the case of a 14-year-old girl with persistent itchy papules in her armpits and pubic area, awaiting diagnosis details.

This case report describes a woman with scalp lichen planopilaris who developed facial papules coinciding with her hair loss condition, raising the question of an associated diagnosis.

This case report details a 31-year-old woman with a subcutaneous nodule on her hand characterized by necrosis and lymphocytic infiltrate.

This chapter reviews various fungal skin diseases affecting cattle but does not report new research findings; it focuses on rare, inherited, and congenital conditions like follicular dysplasia and cutaneous asthenia.

This study reports a case of a child with congenital skin fragility, alopecia, and cardiomyopathy due to compound heterozygous mutations in the DSP gene causing desmoplakin deficiency.

In this study, the staining properties of two types of cysts, epidermal and pilar, were found to differ, supporting their origins from the epidermis and the trichilemmal hair follicle layer, respectively.

This compilation reviews multiple dermatologic studies, reporting findings such as the lack of a psoriasis-susceptibility allele in cluster 17, and highlighting a mouse model for studying hair follicle formation, among others.

This chapter reviews skin manifestations in common rheumatic diseases, particularly those with polyarthritis, and offers a differential diagnosis of erythema nodosum without presenting new research findings.

This study found that acne was the most common dermatological manifestation in Korean women with polycystic ovary syndrome, particularly those with a specific combination of symptoms, showing distinct variations in serum hormonal and metabolic parameters.

This report presents the first known case of ulerythema ophryogenes in a 28-year-old male in Saudi Arabia.

This study identified novel genetic variants related to rare skin and hair disorders, expanding the understanding of conditions like COLED, EV, and monilethrix, including a newly discovered type I keratin gene, KRT31, as a cause for monilethrix.

This case report describes how a misleading presentation of a rash initially resembling vasculitis was ultimately diagnosed as scurvy through histological examination, revealing the importance of dietary history and histopathology in differential diagnosis.

A 70-year-old woman with a rare skin condition improved after treatment with topical steroids and acitretin.

This review analyzed scientific literature and found that dermatological symptoms, such as hirsutism and acne, frequently appear as early indicators of PCOS, reflecting hormonal imbalances and aiding diagnosis of the disorder.

The researchers reported that disrupting the RPGRIP1L gene in mice impaired desmosome function, causing skin blistering, and their findings suggest that PKCβII inhibition could help treat pemphigus.

This case report details a 12-year-old boy from rural south India diagnosed with syringolymphoid hyperplasia, which presented with alopecia and anhidrosis.

This review found that dermatological manifestations often indicate systemic diseases, with endocrine-metabolic disorders, autoimmune diseases, and renal or hepatic conditions frequently linked to specific skin changes, highlighting the diagnostic importance of skin examination in internal medicine and endocrinology.

This study investigated the skin of 12 Baikal seals and identified two main skin pathologies potentially linked to global warming and changes in Lake Baikal's ice regime, including koilocytosis and inflammation associated with a possible viral pathogen.

This report describes a case of widespread Porokeratotic eccrine and hair follicle nevus in a 15-year-old woman with keratitis-ichthyosis-deafness syndrome, involving both eccrine ostia and hair follicle infundibula.

This report documents the first outbreak of a mixed infection of camelpox and dermatophilosis in camels in Iraq, highlighting the need for further study due to the novelty of dermatophilosis in the region.

This study found that infections and eczematous conditions were the most common skin disorders across all ages, with acne vulgaris being notably prevalent in adolescents and young adults.