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http://dx.doi.org/10.3760/cma.j.issn.0529-5807.2013.06.015 | DOI Listing |
Ann Pathol
November 2024
Département de Pathologie, université Paris Est Créteil (UPEC), hôpital Henri-Mondor, AP-HP, 1, rue Gustave Eiffel, 94000 Créteil, France. Electronic address:
Cureus
August 2024
Oncology Surgery, ABC Medical Center, Mexico City, MEX.
This article presents a rare case of nodular mucinosis of the breast, typically manifested as a painless subcutaneous mass in young women. We describe the clinical scenario of a 48-year-old woman who previously underwent benign nodule resection in her 20s at the identical site where nodular mucinosis subsequently developed. This recurrence at the previous resection site underscores the unusual nature of the condition and emphasizes the need for continued vigilance in monitoring patients with a history of such lesions.
View Article and Find Full Text PDFBr J Oral Maxillofac Surg
October 2024
Department of Oral Pathology, Dental School, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Department of Oral Diagnosis, Piracicaba Dental School, Universidade Estadual de Campinas, Piracicaba, SP, Brazil. Electronic address:
Australas J Dermatol
May 2024
Dermatology Department, Birmingham City Hospital, Sandwell and West Birmingham NHS Trust, Birmingham, UK.
Am J Dermatopathol
January 2024
Università Vita-Salute San Raffaele, IRCCS Ospedale San Raffaele, Milano, Italy.
Lichen myxedematosus (LM) is an uncommon cutaneous mucinosis characterized by the deposition of mucin and fibroblast proliferation in the dermis. This condition can be classified into 2 forms: a diffuse/generalized LM, also known as scleromyxedema, associated with monoclonal gammopathy and systemic implications, and a localized form, primarily affecting the skin. Within the localized form, nodular-type LM is a rare variant presenting as firm, skin-colored to pinkish mucinous nodules.
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