Trikofoliküloma
Özet
Trikofoliküloma, kıl folikülünden kaynaklanan, nadir görülen benign (iyi huylu) bir deri eki tümörüdür. Genellikle orta yaşlı erkeklerin baş ve boyun bölgesinde, özellikle yüz ve skalpte deri renginde, kubbe şekilli, asemptomatik soliter bir nodül veya papül olarak izlenir. Etyolojisi tam olarak bilinmemekle birlikte, pluripotent deri hücrelerinden kaynaklandığı düşünülmektedir. Histopatolojik olarak merkezde, yüzeye ostiumlarla açılan ve keratinöz debris ile kıl fragmanları içeren genişlemiş primer infundibulokistik bir yapı barındırır; bu yapıdan çevreye doğru prolifere olan çok sayıda vellus kıl folikülü (sekonder ve tersiyer foliküller) ışınsal olarak uzanır. Sekonder foliküllerde sebase farklılaşma eşlik ettiğinde "sebase trikofoliküloma" olarak adlandırılır. İmmünhistokimyasal incelemede sekonder foliküller CK14 ve bazal tabaka CK15 pozitifliği gösterirken, CK1 ve CK10 ile boyanma izlenmez. Ayırıcı tanısında bazal hücreli karsinom, trikoepitelyoma, pilar kılıf akantomu ve folikülosebase kistik hamartom gibi lezyonlar yer alır. Çok nadir olarak malign transformasyon bildirilmiş olsa da prognozu oldukça iyidir. Tedavisi cerrahi eksizyon ile gerçekleştirilir ve operasyon sonrasında nüks (tekrarlama) olasılığı oldukça düşüktür.
Trichofolliculoma is a rare, benign cutaneous adnexal tumor originating from the hair follicle hamartoma. It typically presents as an asymptomatic, dome-shaped, flesh-colored solitary nodule or papule on the head and neck area, particularly the face and scalp of middle-aged men. Although its etiology remains unclear, it is thought to arise from pluripotent stem cells differentiating toward the hair follicle. Histopathologically, it is characterized by a dilated central primary infundibulocystic follicle opening to the skin surface via ostia, containing keratinous debris and hair fragments. Numerous secondary and tertiary vellus hair follicles radiate from this central cavity into the surrounding dermis. The presence of sebaceous differentiation within these secondary follicles defines the "sebaceous trichofolliculoma" variant. Immunohistochemically, secondary follicles express CK14 and the basal layer shows CK15 positivity, whereas CK1 and CK10 are negative. The differential diagnosis includes basal cell carcinoma, trichoepithelioma, pilar sheath acanthoma, and folliculosebaceous cystic hamartoma. Despite an extremely rare case reporting malignant transformation with perineural invasion, the overall prognosis is excellent. The definitive treatment is complete surgical excision, and recurrence is rarely observed.
Referanslar
Lee H, Kim E. Trichofolliculoma in the Auricle: a case report.Ear,Nose&Throat Journal 2021.doi:10.1177/0145561321995599
Kutzner,H., Kaddu, S.,Kanitakis, J.,Sangüeza, E. J. (2018). Trichofolliculoma. In David E. Elder, Daniela Massi (Eds), WHO Classification of Skin Tumours (4nd ed., pp. 206). Lyon.
Lebe B (2018). Deri Eki Tümörleri. Demirkesen C (Ed). Deri Tümörleri. (316-318) Ankara Nobel Tıp Kitabevleri
Calonje,E., Brenn,T.,Lazar,A. (2020). Tumors of The Hair Follicle. In Thomas Brenn, Alexander J.Lazar (Eds), MCKEE’S Pathology of The Skin (5nd ed., pp.1566-1567).
El-Komy M, Abdelkader H. Congenital Trichofolliculoma: a case report. Dermatology Online Journal 2020, 26 (7). Doi:10.5070/D3267049564
Hosler G,Prenshaw K (2021). Tumors of Cutaneous Appendages. In Patterson,JW (Eds) Weedon’s Skin Pathology (5nd ed,pp 959).
Patterson J. (2012) Cutaneous Appendageal Tumors. In Kevin O.Leslie, Mark R.Wick (Eds). Practical Skin Pathology A Diagnostic Approach ( 3nd ed,pp 362)
Elenitsas R, Rosenbach M et all (2015) Tumors of the Epidermal Appendages. In Elder DE (Eds) Lever’s Histopathology of the skin (11nd ed,pp 1043-1044 )
Crowson A,Magro C,Mihm M (2017) Benign Deri Eki Neoplazileri. Çeviren Aylin Okçu Heper. Deri Biyopsilerinin Yorumu (304-305)
Gökalp H, Gurer M, Alan S. Trichofolliculoma: a rare variant of hair follicle hamartoma: a case report. Dermatology Online Journal 2019 (8):19264. Doi:10.5070/D3198019264
Plewig G. Sebaceous Trichofolliculoma: a case report. J Cutan Pathology 1980, 394-403. Doi:10.1111/j.1600-0560.1980.tb01213.x
Karimzadeh I, Namazi M, Karimzadeh A. Trichoepithelioma: A Comprehensive Review. Acta Dermatovenerol Croat 2018;26(2):162-168
Wu Y. Folliculosebaceous cystic hamartoma or trichofolliculoma? Aspectrum of hamartomatous changes inducted by perifollicular stroma in the follicular epithelium. J Cutan Pathol 2008; 35: 843-848 doi: 10.1111/j.1600-0560.2007.00914.x
Hahm J, Cho S Perifollicular fibroma Journal of the European Academy of Dermatology and Venereology 2006,doi: 10.1111/j.1468-3083. Citations: 8
Nam J, Min J, Lee G A case of perifollicular fibroma. Annals of Dermatology 2011; 23 (2): 236-8. Doi: 10.5021/ad.2011.23.2.236.
Mason A, Shvartsbeyn M, Bosenberg M Perifollicular Fibroma İn Birt-Hogg-Dube Syndrome: an association revisited Journal of Cutaneous Pathology 2012, doi: 10.1111/j.1600-0560.2012.01929.x
Misago N,Kimura T,Narisawa Y Fibrofolliculoma/Tricodiscoma and fibrous papule (perifollicular fibroma/angiofibroma): a revaluation of the histopathological and immunohistochemical features. Journal of Cutaneous Pathology 2009, 46,doi: 10.1111/j.1600-0560.2009.01198.x
Shi H, Xiong J, Gan L. A case of folliculosebaceous cystic hamartoma . Dermatologic Therapy, 2021; 34. Doi: 10.1111/dth.14719
Morse D,Tschen J. A case of folliculosebaceous cystic hamartoma: a rare and clinicallay indistinct lesion . Dermatology Online Journal 2018; 24(7):16 doi:10.570/D3247040921
Shi H, Xiong J, Gan L. A case of folliculosebaceous cystic hamartoma . Dermatologic Therapy, 2021; 34. Doi: 10.1111/dth.14719
Cassarino D, Dadras S, Lindberg M (2016) Trichofolliculoma. In Steven D.Billings (Eds), Diagnostic Pathology Neoplastic Dermatopathology (2nd ed.,pp.594-600).
Phan K, Goyal S, Ahn E Trichofolliculoma of the eyelid: systematic review. Phanet al. Biomedical Dermatology (2020) 4:3 doi:10.1186/s41702-019-0055-x