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Similar Publications
Anetoderma in the Setting of a Hematologic Abnormality and COVID-19 Infection.
Am J Dermatopathol
November 2024
Department of Dermatology, Mayo Clinic, Rochester, MN; and.
Article Synopsis
- * While often considered idiopathic, it has been linked to various disorders, especially those related to blood clotting issues.
- * A case study is presented of a 79-year-old woman with a Factor V Leiden mutation who developed anetoderma following a COVID-19 infection and a thromboembolic event, contributing to existing knowledge on the condition's association with infections and clotting disorders.
Anetoderma after disseminated Mpox.
J Cutan Pathol
June 2024
Dermatology Department, Consorcio Hospital General Universitario de Valencia, Valencia, Spain.
Article Synopsis
- * A 37-year-old male with HIV had over 400 skin lesions resembling those of Mpox, which improved with symptomatic treatment.
- * Eight months later, he developed papular anetoderma in previously affected areas, confirmed by biopsy to show loss of elastic fibers, indicating it was caused by Mpox.
Bullous Pilomatrixoma After COVID-19 Vaccination.
Cureus
December 2022
Department of Internal Medicine, Hospital General "Dr. Agustín O'Horán", Mérida, MEX.
Article Synopsis
- Pilomatrixoma is a benign tumor primarily found in children that originates from hair matrix cells and is one of the most common epithelial tumors in this age group.
- Bullous pilomatrixoma, a rare variant, usually occurs in the upper limbs and is often linked to prior trauma.
- This report focuses on a case where a bullous pilomatrixoma developed rapidly in a patient’s arm one month after receiving the COVID-19 vaccine, raising questions about the nature of the tumor's appearance.
From Morphea to Dermatofibrosarcoma Protuberans.
Acta Dermatovenerol Croat
September 2022
Marija Delaš Aždajić, MD, PhD, Department of Dermatology and Venereology Sestre milosrdnice University Hospital Center, Vinogradska cesta 29 , 10 000 Zagreb , Croatia ;
Article Synopsis
- - Morphea profunda (MP) is a chronic autoimmune disease that leads to restricted skin movement and discomfort, while dermatofibrosarcoma protuberans (DFSP) is a rare, slowly growing tumor that can invade deeper tissues and has a tendency to recur locally but rarely spreads to other parts of the body.
- - A 39-year-old female patient had a brownish lesion diagnosed as MP at 20, which later developed into palpable nodules, leading to further evaluation and a new diagnosis of DFSP after deep biopsy and immunohistochemical analysis.
- - The patient underwent complete surgical removal of the DFSP tumor, followed by additional excision due to inadequate initial margins, and has shown no signs of
Follmann balanitis and anetoderma in secondary syphilis.
Dermatol Reports
June 2022
Dermatology Unit, Ospedale Policlinico San Martino, Genoa.
Article Synopsis
- Syphilitic balanitis of Follmann (FB) is a rare form of primary syphilis first identified in 1948, presenting in various ways from painful swelling to asymptomatic hardening of the glans.
- A case study highlights a patient with FB who also exhibited anetoderma, a feature of secondary syphilis.
- This is the first documented instance of these two conditions occurring together, suggesting a unique clinical relationship.
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