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Gotowe bibliografie tematyczne / Trichoepithelioma multiplex

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Gotowa bibliografia na temat „Trichoepithelioma multiplex”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Trichoepithelioma multiplex"

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Centurión, Santiago A., Robert A. Schwartz, and W. Clark Lambert. "Trichoepithelioma Papulosum Multiplex." Journal of Dermatology 27, no. 3 (2000): 137–43. http://dx.doi.org/10.1111/j.1346-8138.2000.tb02139.x.

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Igawa, Ken, Toshiyuki Yamamoto, and Kiyoshi Nishioka. "Vellous Hair in Trichoepithelioma papulosum multiplex." Dermatology 209, no. 4 (2004): 338–39. http://dx.doi.org/10.1159/000080860.

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MAEKAWA, Tomoko, Yumiko KAKU, Kayo HARADA, and Kazunori URABE. "A Case of Trichoepithelioma Multiplex in an Infant." Nishi Nihon Hifuka 76, no. 6 (2014): 533–34. http://dx.doi.org/10.2336/nishinihonhifu.76.533.

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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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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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Tenea, Daniela. "Trichoepithelioma Multiplex: A Study of the Relationship between the Anatomical Location and the Histopathological Features." British Journal of Medicine and Medical Research 3, no. 4 (2013): 1015–29. http://dx.doi.org/10.9734/bjmmr/2013/2930.

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Dr., DS Gupta, Saubhagya S. Agrawal Dr., Aashita jain Dr., Shilpi Shrivastava Dr., Nakul Chaudhary Dr., and Deepika Saini Dr. "A Rare Case of Trichoepithelioma on Unusual Location." A Rare Case of Trichoepithelioma on Unusual Location 8, no. 11 (2023): 3. https://doi.org/10.5281/zenodo.10212719.

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Purpose: Trichoepithelioma is a very rare benign tumor of the skin. Trichoepitheliomas originate in hair follicles and occur in the head and neck. It is found on the scalp, nose, and forehead, but very rarely on the hairless part of the upper lip. Therefore, removal of trichoepithelioma was performed to improve facial aesthetics, which was the patient's primary concern.Material& methods/ Case description: An adult male patient reported to the department with the solitary nodular lesion on the non-hair bearing area of left upper lip.Result: Post-op after 3 months there was no scar formation

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Dissanayaka, D. W. V. N., D. K. B. Dassanayaka, and P. R. Jayasooriya. "Clinical, Histopathological, and Management Challenges of Multiple Familial Trichoepithelioma: A Case Report of a Patient Presenting with Multiple Facial Papules." Case Reports in Dentistry 2020 (September 9, 2020): 1–6. http://dx.doi.org/10.1155/2020/5648647.

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Trichoepitheliomas (TE) are benign skin tumours of the pilosebaceous apocrine unit with follicular differentiation. Multiple familial trichoepithelioma (MFT) is a considerably rare condition inherited in an autosomal dominant pattern. We present a case of a 15-year-old male who presented with multiple papulo-nodular lesions in the central face and a family history of a similar type of lesions from his mother. Significance of consideration of various clinical differential diagnoses with serious pathological outcomes, strategies followed in the diagnosis including histopathological evaluation ai

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Gaydina, Tatiana A., Anton S. Dvornikov, Polina A. Skripkina, Olga I. Patsap, and Anastasiia A. Buianova. "Differential diagnosis of Brooke–Spiegler syndrome in a young woman with multiple trichoepitheliomas." Russian Journal of Skin and Venereal Diseases 25, no. 6 (2023): 5–16. http://dx.doi.org/10.17816/dv112260.

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BrookeSpiegler syndrome (Brooke-Spiegler syndrome; OMIM #605041) is a rare, autosomal dominant inherited monogenic disease caused by mutations in gene CYLD with its different penetrance. It is clinically manifested by the development of multiple neoplasms of skin appendages such as spiradenoma, cylindroma, spiradenocylindroma and trichoepithelioma. Several phenotypic variants with mutations in gene CYLD have been described in the scientific literature. They are classic BrookeSpiegler syndrome; multiple familial trichoepithelioma syndrome (multiple trichoepitheliomas without cylindromas,

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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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Części książek na temat "Trichoepithelioma multiplex"

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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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"Trichoepithelioma papulosum multiplex." In Dermatology Therapy. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/3-540-29668-9_2729.

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"11.5 Multiple Trichoepitheliome." In Dermatologie von Fall zu Fall, edited by Lutz Kowalzick and Gunnar Wagner. Georg Thieme Verlag, 2013. http://dx.doi.org/10.1055/b-0034-57888.

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