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Gotowe bibliografie tematyczne / Familial multiple trichoepitheliomas

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Gotowa bibliografia na temat „Familial multiple trichoepitheliomas”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Familial multiple trichoepitheliomas"

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N., Priyadharshini, Harini Irri, and Sathyanarayanan R. "Multiple familial trichoepitheliomas: a case report." International Journal of Research in Dermatology 7, no. 3 (2021): 487. http://dx.doi.org/10.18203/issn.2455-4529.intjresdermatol20211719.

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<p class="abstract">Trichoepithelioma is a rare benign adnexal tumor that differentiates towards the folliculo-sebaceous-apocrine unit (trichoblast). It may present as solitary non-familial lesion or multiple lesions as a part of autosomal dominant inherited syndrome known as multiple familial Trichoepithelioma. Multiple familial trichoepithelioma is a relatively rare, disfiguring, benign adnexal neoplasm diagnosed by centrofacial distribution of papules and nodules, positive family history, related histopathological findings and can rarely undergo malignant transformation. Treatment is

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Tiodorović, Danica, and Miljan Krstić. "Clinical, Histological and Dermoscopic Findings in Familial Cylindromatosis: a Report of Two Cases." Serbian Journal of Dermatology and Venereology 7, no. 2 (2015): 75–82. http://dx.doi.org/10.1515/sjdv-2015-0008.

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Abstract Cylindromas are benign appendage tumors mainly found on the scalp, but they can occur on any hair-bearing skin. Mutations in the cylindromatosis (CYLD) gene, a tumor suppressor gene located on chromosome 16q12–13, are responsible for multiple cylindromas, which are usually inherited in an autosomal dominant way, as in familial cylindromatosis and Brooke-Spiegler syndrome. The latter is characterized by the presence of multiple cylindromas, multiple trichoepitheliomas and spiradenomas. Based on genetic studies and the identification of heterozygous mutations in the same CYLD gene in fa

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Clarke, Jennie, Michael Ioffreda, and Klaus F. Helm. "Multiple Familial Trichoepitheliomas." American Journal of Dermatopathology 24, no. 5 (2002): 402–5. http://dx.doi.org/10.1097/00000372-200210000-00005.

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Rao Venkata Mahipathy, Surya Rao, Narayanamurthy Sundaramurthy, Vimal Chander Rajamanohar, Alagar Raja Durairaj, and Manimaran Ramachandran. "Giant solitary trichoepithelioma masquerading as basal cell carcinoma." International Surgery Journal 5, no. 7 (2018): 2649. http://dx.doi.org/10.18203/2349-2902.isj20182790.

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Trichoepithelioma is a rare benign adnexal tumour which can be of solitary non-familial type or multiple familial trichoepitheliomas. Here authors describe a middle-aged patient who presented with a swelling of the left nasolabial region diagnosed clinically as a basal cell carcinoma but proved to be a giant solitary trichoepithelioma (GST) following histopathological examination. This case is presented due to the rarity and the difficulty encountered in diagnosis of the case.

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Amaaoune, Fatima, Wassima Zidane, Mohamed Aksim, Maryem Aboudourib, Ouafa Hocar, and Said Amal. "Multiple non-familial trichoepitheliomas: A rare case and a review of the literature." Our Dermatology Online 14, no. 3 (2023): 307–10. http://dx.doi.org/10.7241/ourd.20233.17.

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Trichoepitheliomas are benign tumors of follicular origin often appearing in childhood or early adolescence. They present as small, firm papulonodular lesions of normal skin color or translucent. The lesions gradually increase in size and then stabilize. They sit electively on the face, mainly on the nasolabial folds, forehead, chin, and cheeks, and sometimes on the scalp and neck. Trichoepitheliomas may be divided into three subgroups: multiple familial trichoepitheliomas, solitary non-hereditary trichoepitheliomas, and desmoplastic trichoepitheliomas. Non-familial multiple trichoepitheliomas

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Shapiro, P. E. "Familial multiple desmoplastic trichoepitheliomas." Archives of Dermatology 127, no. 1 (1991): 83–87. http://dx.doi.org/10.1001/archderm.127.1.83.

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Shapiro, Philip E. "Familial Multiple Desmoplastic Trichoepitheliomas." Archives of Dermatology 127, no. 1 (1991): 83. http://dx.doi.org/10.1001/archderm.1991.01680010093015.

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Amaaoune, F., W. Zidane, M. Akssim, M. Aboudourib, O. Hocar, and S. Amal. "Multiple Nonfamilial Trichoepitheliomas: A Rare Case with Review of the Literature." Scholars Journal of Medical Case Reports 11, no. 05 (2023): 801–4. http://dx.doi.org/10.36347/sjmcr.2023.v11i05.012.

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Trichoepitheliomas are benign tumors of follicular origin and often appear in childhood or early adolescence. They present as small, firm papulonodular lesions of normal skin color or translucent. The lesions gradually increase in size and then stabilize. They sit electively on the face, mainly in the nasolabial folds, on the forehead, chin, and cheeks, and sometimes on the scalp and neck. Trichoepitheliomas can be divided into three subgroups: multiple familial Trichoepitheliomas, solitary non-hereditary Trichoepitheliomas, and desmoplastic Trichoepitheliomas. Nonfamilial multiple trichoepith

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Capusan, Tania M., Lucero Noguera‐Morel, Elena Bueno‐Martínez, et al. "Multiple familial trichoepitheliomas: Ultrasonographic findings." Skin Research and Technology 26, no. 1 (2019): 137–39. http://dx.doi.org/10.1111/srt.12746.

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Sood, Samriti, Mudita Gupta, Reena Kumari Sharma, and Manju Rao. "Multiple Non- Familial Trichoepitheliomas in a NineYear Child." Nepal Journal of Dermatology, Venereology & Leprology 17, no. 1 (2019): 76–78. http://dx.doi.org/10.3126/njdvl.v17i1.21119.

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Trichoepitheliomas are rare benign tumours of poorly differentiated trichogenic origin. They present as translucent lesions most commonly on centrofacial regions. Solitary lesions are seen in sporadic cases while multiple lesions are inherited in autosomal dominant pattern. We present a 9 year old child with multiple trichoepitheliomas at classical sites with none of the other family members involved.

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Części książek na temat "Familial multiple trichoepitheliomas"

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Oette, Mark, Marvin J. Stone, Hendrik P. N. Scholl, et al. "Multiple Familial Trichoepithelioma." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_1201.

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