5 citations
,
January 2021 in “Indian Journal of Pathology and Microbiology” 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.
1 citations
,
January 2021 in “Figshare” 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.
1 citations
,
January 2007 in “The Internet Journal of Dermatology” This case report describes a solitary nasal fibrofolliculoma in a 60-year-old male and reviews existing literature, indicating its rare occurrence and potential link with Birt-Hogg-Dube syndrome.
33 citations
,
May 2015 in “JAMA Dermatology” This study identifies comedonal or cystic fibrofolliculomas as novel diagnostic clues for earlier recognition of Birt-Hogg-Dube syndrome, potentially facilitating timely surveillance of associated systemic complications.
16 citations
,
March 2011 in “Ophthalmic genetics” This case report documents a 63-year-old with Birt-Hogg-Dubé Syndrome who developed choroidal melanoma alongside multiple lid folliculomas, marking the first known association of these conditions.
30 citations
,
October 1994 in “Journal of Cutaneous Pathology” This article describes a case of multiple perifollicular fibromas and suggests that cases previously reported as such might actually be instances of Birt‐Hogg‐Dubé syndrome.
7 citations
,
September 2013 in “Familial cancer” This review discusses recent insights into Birt–Hogg–Dube syndrome, including the functions of the FLCN gene and clinical recommendations for screening and treatment, but it reports no new experimental results.
4 citations
,
January 2019 in “Journal of cutaneous pathology” This study found that phospho-S6 is strongly expressed in malignant hair follicle tumors but only patchily in a minority of benign tumors, indicating a potential marker for distinguishing between the two.
October 2023 in “Research Review” This source describes the development, structure, and types of skin appendage tumors, noting both benign and malignant forms, potential associations with syndromes, and categories based on follicular differentiation.
December 2012 in “Expert review of dermatology” This review summarizes current knowledge about Birt–Hogg–Dubé syndrome, discussing recent findings on its pathogenesis and treatment, but reports no new clinical results; the authors emphasize understanding its cutaneous manifestations.
January 2013 in “Kidney international” This report describes a clinical case of a 38-year-old man diagnosed with Birt-Hogg-Dubé syndrome, confirmed by genetic testing, highlighting the presentation of multiple renal tumors and bilateral lung cysts.
16 citations
,
March 2005 in “Journal of The American Academy of Dermatology” This report describes a case of Birt-Hogg-Dube syndrome with manifestations including multiple fibrofolliculomas, acrochordons, and renal oncocytoma.
3 citations
,
March 2005 in “Journal of the American Academy of Dermatology” This case report describes a patient with Birt-Hogg-Dube syndrome exhibiting multiple fibrofolliculomas, acrochordons, and renal oncocytoma.
April 2025 in “Indian Journal of Dermatology” In this case report, a 24-year-old male with a translucent nodule in the left nasolabial fold was diagnosed with a solitary fibrofolliculoma with cystic changes upon histopathology, emphasizing the rarity and potential for misdiagnosis of these benign cutaneous tumors.
6 citations
,
June 2010 in “Dermatologica Sinica” 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.
June 2022 in “IP Indian journal of clinical and experimental dermatology” This case report discusses a benign trichofolliculoma in a 40-year-old woman, confirmed through histopathological examination with no recurrence noted during a one-year follow-up period.
18 citations
,
January 2013 in “Dermatology Online Journal” This case report describes a 19-year-old woman with typical clinical and histopathological findings of trichofolliculoma, a rare hair follicle hamartoma usually located on the face or scalp.
January 2022 in “Journal of clinical and diagnostic research” This case report describes an uncommon occurrence of trichofolliculoma in a 64-year-old male, which was easily treated through simple excision.
July 2025 in “Clinical Dermatology Review” In this case report, researchers observed multiple trichofolliculomas in family members, noting this as a rare manifestation of typically singular hair follicle hamartomas.
June 2021 in “Scholars journal of applied medical sciences” This article reviews the literature on trichofolliculoma, a rare benign hair follicle tumor, and provides an observational report, noting the lack of consensus on treatment.
19 citations
,
September 2016 in “Journal of the European Academy of Dermatology and Venereology” This article is a letter discussing a clinicopathologic study of 90 cases of trichofolliculoma and reports no new results.
September 2022 in “TURKDERM” This article reports an unprecedented case of trichofolliculoma in the gluteal area, previously unreported in English literature.
December 2025 in “SAS Journal of Medicine” This case report highlights the importance of considering trichofolliculoma in the differential diagnosis of scalp lesions, with histopathological examination essential for accurate diagnosis.
September 2025 in “Egyptian Journal of Dermatology and Venerology” This case study described the diagnosis of a trichofolliculoma in a 56-year-old woman, emphasizing its dermoscopic features and histological aspects that confirmed the tumor type, with no recurrence observed after excision.
4 citations
,
August 1991 in “The Journal of Dermatology” 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.
1 citations
,
January 2022 in “Clinical dermatology review” This case report describes a 26-year-old male patient with trichofolliculoma, highlighting dermoscopic features that aid its diagnosis and distinct characteristics from other similar lesions.
January 2025 in “International Journal of Dermatology” This case report describes a patient with eruptive tumor of follicular infundibulum, emphasizing the need for dermatologists to include it in the differential diagnosis of acquired facial hypopigmentation.
5 citations
,
March 2015 in “Indian Journal of Dermatology” This report describes a rare case of multiple trichofolliculomas on the face, which clinically resembled multiple trichoepitheliomas.
81 citations
,
August 1979 in “Archives of Dermatology” This case report describes a trichofolliculoma with perineural invasion, highlighting a rare and clinically significant finding in a typically benign hair follicle tumor.
2 citations
,
June 2022 in “Life” This case report reviews panfolliculoma, a rare benign follicular tumor, highlighting its occurrence and characteristics, and emphasizes the importance of accurate histopathological differentiation to avoid misdiagnosis.