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This case series observed that solitary fibrofolliculoma is a rare lesion that can affect the eyelids, requiring histological examination for accurate diagnosis due to its nonspecific clinical appearance.

This case report describes a rare occurrence of a solitary fibrofolliculoma in the right lower eyelid of a 50-year-old man, confirmed through histopathological examination.

This study observed a high incidence of hemangioma rubi on the scalp in older adults, which had not been previously reported in the literature.

This report describes three cases of feline exudative dermatitis in neutered European cats, associated with lymphangiosarcoma, confirmed by histopathological and ultrastructural findings.

This study found that postmenopausal women in Argentina with frontal fibrosing alopecia had a higher average age of diagnosis than previously reported, with similar clinical features to international cases.

This case report discusses a patient with VHL-associated paraganglioma, highlighting the importance of genetic testing and monitoring in those with VHL disease, due to high mutation penetrance and associated risks.

This report describes a rare case of angiokeratomas on both the upper eyelids and scrotum, adding to the limited literature on eyelid occurrences and discussing potential causes.

This case report describes a 22-year-old woman with a nevoid plaque termed localized follicular hamartoma, characterized by skin-colored papules and specific cellular and structural features.

A man had a non-cancerous, fast-growing skin lump on his arm that was removed with surgery.

This study identified that bone marrow-derived CD34⁺ cells act as fibroblast progenitors to enhance tissue regeneration in ischemic limbs by promoting angiogenesis through interactions with macrophages.

This study reports that in a case of benign Brenner tumor, elevated androgens may originate from luteinized stromal cells, as these cells do not convert androgen to estrogen due to suppressed aromatase biosynthesis.

This case report describes a 61-year-old female with hyperandrogenic symptoms, where an ovarian hemangioma with stromal luteinization was identified and surgically removed, resulting in improved symptoms.

This case report describes a giant pigmented tumor of the scalp in a 47-year-old woman and suggests a possible dual origin involving neural crest differentiation.

In this case study, a 23-year-old man initially suspected of having minoxidil-induced pericarditis was ultimately diagnosed with cardiac angiosarcoma, highlighting the need to consider malignancy in cases of recurrent pericarditis in young adults.

This case report describes the dermoscopic features of two cases of the tumor of the follicular infundibulum, contributing new insights as they had not been previously detailed in the literature.

This case study speculates on a potential link between angiosarcoma and hair follicle miniaturization-induced alopecia in an elderly woman, suggesting possible directions for new treatment research.

This report describes two male patients with frontal fibrosing alopecia, a lymphocytic scarring hair loss condition often seen in postmenopausal women, highlighting its occurrence in men and its manifestation around the frontal hairline and other body areas.

This review highlights the potential of amphiregulin as a therapeutic target, noting its role in both fibrotic and malignant diseases, and discusses promising early findings but reports no new clinical results.

This report highlights a case where intralesional cidofovir successfully treated squamous cell carcinoma without systemic toxicity, suggesting it may be a viable alternative to surgical excision.

In this report, two pediatric cases of solitary basaloid follicular hamartoma, a rare benign skin malformation often misdiagnosed, were documented using dermoscopy, highlighting its clinical diversity and the need for accurate diagnosis.

This case report documents the presentation and diagnosis of a rare bullous pilomatrixoma in a 20-year-old female using fine needle aspiration cytopathology, highlighting diagnostic challenges and features.

This case report describes a rare pedunculated follicular hamartoma on the nasal septum of a 77-year-old Japanese male, emphasizing its unique clinical and pathological features.

A case study reported a 15-year-old boy with a diagnosis of giant folliculosebaceous cystic hamartoma on his right buttock, characterized by malformed hair follicles and sclerotized collagen.

In this study, researchers reported two cases of the rare and benign follicular tumor called panfolliculoma, highlighting its differentiation across all hair follicle components, which is distinct from similar conditions like trichofolliculoma.

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.

This case report details a 26-year-old woman with a rare large functional adrenal myelolipoma, characterized by elevated hormone levels and requiring surgical intervention.

This study reports on a unique clinical presentation of folliculotropic mycosis fungoides in a 60-year-old man, highlighting complexities in diagnosis due to dense histiocytic infiltration, which led to xanthoma formation before treatment, and obscured lymphomatous features.

This article reviews potential causes for angiolymphoid hyperplasia with eosinophilia, a benign vascular tumor often found in middle-aged adults, and reports no new clinical findings.

This case report describes a 16-year-old girl with severe generalized gingival fibromatosis and hypertrichosis, who underwent successful treatment through gingivectomy, with uneventful healing observed over an eight-month follow-up.

A rare benign scalp tumor in an infant requires surgical removal.