Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/44322
Title: Gorlin-Goltz Syndrome and Neoplasms: A Case Study
Authors: Lopes, Nilza Nelly Fontana [UNIFESP]
Caran, Eliana Maria Monteiro [UNIFESP]
Lee, Maria Lúcia de Martino [UNIFESP]
Silva, Nasjla Saba da [UNIFESP]
Rocha, Andre Caroli
Macedo, Carla R. D. [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
Keywords: Gorlin syndrome
odontogenic keratocysts
basal cell carcinoma
medulloblastoma
acute myeloid leukemia
Issue Date: 1-Dec-2010
Publisher: Journal Pedodontics Inc
Citation: Journal Of Clinical Pediatric Dentistry. Birmingham: Journal Pedodontics Inc, v. 35, n. 2, p. 203-206, 2010.
Abstract: Gorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expressivity. It is characterized by facial dysmorphism, skeletal anomalies, multiple basal cell carcinomas, odontogenic keratocysts (OKC), palmar and plantar pits, bifid ribs, vertebral anomalies and a variety of other malformations. Various neoplasms', such as medulloblastomas, meningiomas, ovarian and cardiac fibromas are also found in this syndrome. Objective: To describe a twelve-year-old patient with Gorlin-Goltz syndrome, with basal cell carcinomas and promyelocytic leukemia developed after receiving craniospinal radiation for a medulloblastoma. Mild ribs as well as mandibular and maxillar OKC were also diagnosed. Conclusion: The patient with Gorlin-Goltz syndrome should receive close follow-up for early detection of malformations and malignant neoplasias.
URI: http://repositorio.unifesp.br/11600/44322
ISSN: 1053-4628
Other Identifiers: https://doi.org/10.17796/jcpd.35.2.x01248284w166485
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