Academic literature on the topic 'Pilomatricoma'

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Journal articles on the topic "Pilomatricoma"

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Harsha, Muvva Sri, Rajesh Goud E., and Srikanth Jakkula. "Benign proliferative pilomatricoma over sternum: a rare case." International Surgery Journal 5, no. 7 (2018): 2657. http://dx.doi.org/10.18203/2349-2902.isj20182792.

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Pilomatricoma is a benign, uncommon, subcutaneous tumor arising from the outer root sheath cell or hair matrix cells. Pilomatrixoma, benign calcifying epithelioma of Malherbe, trichomatricoma are synonyms for pilomatricoma. They occur mostly on head, neck and upper limb extremities. Histologically they classically consist of peripheral basiloid cells and central enucleated ghost or shadow cells. Malignant changes are rare in pilomatricomas. However, the proliferative variety is aggressive and considered to be precursor of malignancy. Here we present a case of benign proliferative pilomatricoma
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Eng, Renee K., Ahmed Shehabeldin, Megan Ketcham, Parul Shah, Seema Mullick, and Jae Y. Ro. "Multiple pilomatricomas: Recurrent skin nodules in myotonic dystrophy." Case Reports in Clinical Pathology 7, no. 1 (2020): 34. http://dx.doi.org/10.5430/crcp.v7n1p34.

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Pilomatricoma is a relatively uncommon benign tumor derived from the matrix of hair follicles. Multiple pilomatricomas may arise sporadically or in association with other disease entities. These entities include myotonic dystrophy type-1, a multisystem disorder that confers increased susceptibility to developing neoplasms, as well as familial adenomatous polyposis-related syndromes (including Gardner syndrome) and others. Here we present two case reports of multiple pilomatricomas that were initially misidentified clinically. We discuss pilomatricoma as a differential diagnosis of multiple ski
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Chessa, Marco Adriano, Maria Francesca Baracca, Alice Nadia Rossi, et al. "Pilomatricoma: Clinical, Dermoscopic Findings and Management in 55 Pediatric Patients and Concise Review of the Literature With Special Emphasis on Dermoscopy." Dermatology Practical & Conceptual 14, no. 2 (2024): e2024140. http://dx.doi.org/10.5826/dpc.1402a140.

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Introduction: Pilomatricoma is a benign adnexal dermal or subcutaneous tumor derived from immature hair matrix cells. Objectives: The aim of our study is to evaluate clinical and dermoscopic features of pilomatricomas, with a specific focus on pediatric lesions, and to provide a concise review of the existing literature. Methods: A single-center retrospective study was undertaken on 55 patients with a histopathological diagnosis of pilomatricoma referred to the Dermatology Unit, University of Bologna, Bologna, Italy, between 2005 and 2023. Pilomatricomas were retrospectively evaluated relying
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Bouabdella, Sara, Afaf Khouna, Siham Dikhaye, and Nada Zizi. "Isolated pilomatricoma of the arm: A case and a review of the literature." Our Dermatology Online 13, no. 1 (2022): 86–88. http://dx.doi.org/10.7241/ourd.20221.21.

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Pilomatricoma is a relatively rare tumor of the skin derived from primitive basal cells of the epidermis that differentiate into hair matrix cells. These tumors appear as solitary, firm nodules, showing a normal to pearl white epidermis. Its most frequent locations are the head and neck, while involvement of the upper extremities is relatively uncommon. Herein, we present the case of a seventeen-year-old female with pilomatricoma of the arm and review the literature regarding pilomatricomas of the upper extremities. The diagnosis of pilomatricoma is confirmed histologically and its treatment i
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Chakrabarti, Indranil. "Ossifying pilomatricoma: A rare entity." IP Archives of Cytology and Histopathology Research 7, no. 3 (2022): 202–4. http://dx.doi.org/10.18231/j.achr.2022.045.

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Pilomatricomas are rare benign skin adnexal tumors usually occurring in the head, neck or upper extremities of children and young adults. Ossifying pilomatricoma is a still rarer entity. Here, a case of a 22-year-old lady is reported, who presented with a firm to hard swelling in the right side of the neck. Histopathological examination of the resected specimen showed features of ossifying pilomatricoma with the formation of bone marrow elements. The patient was free of recurrence on 6-month follow-up. The case highlights a rare entity with characteristic histopathological features.
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D, Yogesh, Rashmi R. Mallya, Zigu S. Krishn, and K. Yashwanth Reddy. "Multiple malherbe’s calcifying epithelioma: A case report." IP Indian Journal of Clinical and Experimental Dermatology 8, no. 2 (2022): 135–37. http://dx.doi.org/10.18231/j.ijced.2022.029.

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Pilomatricoma, is an appendageal tumour of the skin usually seen in head and neck area. They are usually solitary, derived from the ectoderm and arise from the outer root sheath cells of the hair follicle. Multiple pilomatricomas are rare. We present a case of multiple pilomatricomas over the arm of a 13 year old girl.
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Sparling, Kennedy, and Christina Harview. "Pilomatricoma on the Abdomen with Overlying Striae Distensae: A Unique Presentation." SKIN The Journal of Cutaneous Medicine 8, no. 1 (2024): 1287–90. http://dx.doi.org/10.25251/skin.8.1.12.

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Pilomatricomas are benign neoplasms of the hair follicle. Alterations in the skin overlying pilomatricomas are rarely reported, and there are no reports with overlying striae distensae. We present an unusual case of pilomatricoma with overlying striae distensae on the flank of a young man and report its clinical findings. Recognition of this unique presentation of pilomatricomas is important for timely diagnosis and improved patient care, as these lesions have the potential for malignant transformation into pilomatrix carcinoma.
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Cavalcante, Mateus Barros, Éwerton Daniel Rocha Rodrigues, Caio Pimenteira Uchôa, et al. "Abordagem cirúrgica de pilomatricoma – relato de caso." Research, Society and Development 9, no. 10 (2020): e839108244. http://dx.doi.org/10.33448/rsd-v9i10.8244.

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Pilomatricoma ou epitelioma calcificante de Malherbe é uma neoplasia cutânea benigna rara, com origem nas células da matriz do folículo piloso que surge na maioria dos casos durante a infância ou adolescência. Clinicamente apresentam-se frequentemente como nódulos assintomáticos, com coloração geralmente semelhante à pele normal, localizados predominantemente na cabeça, pescoço ou extremidades superiores, de consistência habitualmente dura, crescimento lento e na maioria dos casos solitárias. A excisão cirúrgica é geralmente recomendada para os pilomatricomas, para prevenir o seu crescimento o
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Yasin, Rafeya, Sameen Afzal, Ghazi Zafar, and Samina Zaman. "Pilomatricoma with extensive ossification and marrow formation: a case report and review of literature." Pakistan Journal of Pathology 36, no. 1 (2025): 63–65. https://doi.org/10.55629/pakjpathol.v36i1.828.

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Pilomatricomas are follicular cystic neoplasms involving the dermis and subcutaneous tissue and have a benign behavior. Clinically they may present as hard papules or nodules. Histologically, they comprise of mummified cells, fibrillary bodies and trichohyaline granules. Excision is usually curative. Here we present a case of female patient with a lesion on back that turned out to be pilomatricoma but with extensive ossification.
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Leblebici, Cem, Begüm Yeni, Ozan Erdem, Ayşe Esra Koku Aksu, Erol Rüştü Bozkurt, and Cuyan Demirkesen. "Superficial variant of pilomatricoma, so‐called pilomatricomal horn." Journal of Cutaneous Pathology 46, no. 11 (2019): 801–4. http://dx.doi.org/10.1111/cup.13495.

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Dissertations / Theses on the topic "Pilomatricoma"

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Rumayor, Piña Alicia 1984. "Análise comparativa das características histológicas e imunoistoquímicas do pilomatricoma, craniofaringioma e tumor odontogênico cístico calcificante." [s.n.], 2013. http://repositorio.unicamp.br/jspui/handle/REPOSIP/288359.

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Orientador: Oslei Paes de Almeida<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba<br>Made available in DSpace on 2018-08-22T06:50:59Z (GMT). No. of bitstreams: 1 RumayorPina_Alicia_M.pdf: 5492242 bytes, checksum: d72d6dba44229ac2e8e3d662cfee7879 (MD5) Previous issue date: 2013<br>Resumo: Pilomatricoma (PM), craniofaringioma (CF) e tumor odontogênico cístico calcificante (TOCC) são tumores que compartilham uma característica histopatológica marcante, a presença de células fantasmas. O objetivo deste trabalho foi analisar e comparar as cara
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Books on the topic "Pilomatricoma"

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Sybert, Virginia P. Tumors/Hamartomas. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780195397666.003.0010.

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Basal Cell Nevus Syndrome – Bathing Trunk Nevus – Cowden Disease – Cylindromatosis – Dysplastic Nevus Syndrome – Epidermal Nevus – Gardner Syndrome – Hereditary Keratoacanthomas – Infantile Myofibromatosis – Multiple Endocrine Neoplasia Types 1, 2A, and 2B/3 – Multiple Leiomyomatosis – Pilomatricoma – Proteus Syndrome – Sebaceous Nevus Syndrome – Tumoral Calcinosis
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Sybert, Virginia P. Tumors/Hamartomas. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190276478.003.0010.

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Chapter 10 covers Basal Cell Nevus Syndrome, Cowden Syndrome, Cylindromatosis, Dysplastic Nevus Syndrome, Epidermal Nevus, Gardner Syndrome, Giant congenital nevocytic nevus, Hereditary Keratoacanthomas, Hereditary Leiomyomatosis and renal cell cancer, Infantile Myofibromatosis, Multiple Endocrine Neoplasia Types 1, 2A, and 2B/3, Pilomatricoma, Proteus Syndrome, Sebaceous Nevus Syndrome, and Tumoral Calcinosis. Each condition is discussed in detail, including dermatologic features, associated anomalies, histopathology, basic defect, treatment, mode of inheritance, prenatal diagnosis, and diffe
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Book chapters on the topic "Pilomatricoma"

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Kazakov, Dmitry V. "Pilomatricoma." In Encyclopedia of Pathology. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-30006-1_463.

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Requena, Luis, and Omar Sangüeza. "Pilomatricoma." In Cutaneous Adnexal Neoplasms. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-45704-8_52.

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Braun-Falco, Markus, Henry J. Mankin, Sharon L. Wenger, et al. "Pilomatricoma." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_3364.

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Hundeiker, M., and A. Lippold. "Pilomatricome: Entwicklung und Therapie." In Das Basaliom. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-77908-4_8.

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"Pilomatricoma." In Encyclopedia of Genetics, Genomics, Proteomics and Informatics. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_12872.

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"Pilomatricoma." In Dermatology Therapy. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/3-540-29668-9_2136.

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"Pilomatricoma." In Pediatric Dermatology and Dermatopathology. CRC Press, 2001. http://dx.doi.org/10.1201/b14322-99.

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"Pilomatricoma." In Diagnostic Pathology: Pediatric Neoplasms. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-323-54806-9.50015-x.

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"Pilomatricoma." In Pediatric Dermatology, 4th ed. American Academy of PediatricsItasca, IL, 2021. http://dx.doi.org/10.1542/9781610024594-80.

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Sacchidanand, S., AS Savitha, and K. Shilpa. "Pilomatricoma." In Snapshots in Dermatology. Jaypee Brothers Medical Publishers (P) Ltd., 2013. http://dx.doi.org/10.5005/jp/books/11874_165.

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Conference papers on the topic "Pilomatricoma"

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Quiñonez, M. A., and M. E. Vijil. "Pulmonary Sarcoidosis and Pilomatricoma." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a1548.

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MAURIZ, TALLYS CARVALHO, LILLIAN MARIA FERNANDES DE CASTRO, AGAMENON FERNANDES NETO, GABRIEL BARBOZA DE ANDRADE, VICTOR CARVALHO ALVES, and THIAGO PEREIRA DINIZ. "PILOMATRICOMA: UM RELATO DE CASO." In ANAIS DO III CONGRESSO BRASILEIRO MéDICO ACADêMICO | XI CONGRESSO NORDESTINO MéDICO ACADêMICO | XXVII CONGRESSO MéDICO ACADêMICO. Galoa, 2021. http://dx.doi.org/10.17648/comapi-2021-139471.

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Luelmo, María Isabel, Francisco López, Iker Chouza, Marta de Santiago, Andrea Nieto, and Lucía María Sangro. "Diagnóstico ecográfico y manejo del pilomatricoma en atención primaria." In 31 Congreso Nacional de Medicina General y de Familia. Grupo Pacífico, 2025. https://doi.org/10.48158/semg25-133.

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