دورية أكاديمية

Acrokeratosis Paraneoplastica Associated with Cervical Squamous Cell Carcinoma

التفاصيل البيبلوغرافية
العنوان: Acrokeratosis Paraneoplastica Associated with Cervical Squamous Cell Carcinoma
المؤلفون: Bryan Squires, Steven D. Daveluy, Michael C. Joiner, Newton Hurst, Michael Bishop, Steven R. Miller
المصدر: Case Reports in Dermatological Medicine, Vol 2016 (2016)
بيانات النشر: Hindawi Limited, 2016.
سنة النشر: 2016
المجموعة: LCC:Dermatology
مصطلحات موضوعية: Dermatology, RL1-803
الوصف: Background. Acrokeratosis paraneoplastica, or Bazex syndrome, is a paraneoplastic syndrome characterized by cutaneous psoriasiform lesions with associated acral erythema and scale, as well as nail changes, including onycholysis and ungual dystrophy. Its most advanced, severe form involves the trunk, elbows, and knees. It is typically associated with upper aerodigestive tract malignancies in males. Rare cases associated with gynecological cancers have been reported, including uterine adenocarcinoma, as well as ovarian and vulvar squamous cell carcinomas. Cutaneous manifestations often precede cancer diagnosis. In most reported cases, skin changes resolve when the underlying malignancy is adequately treated. Main Observations. We present the case of a 56-year-old female diagnosed with acrokeratosis paraneoplastica following the discovery of FIGO stage IIB cervical squamous cell carcinoma (SCC). Scaling, hyperpigmentation, xerosis, and fissuring were noted on the patient’s hands, feet, legs, arms, and lower back. Pitting was noted on her fingernails. Her cervical cancer was successfully treated with chemoradiotherapy, after which her cutaneous lesions persisted for two months before resolving. Conclusions. The presentation of acrokeratosis paraneoplastica in this context is atypical. Reports of associations with gynecological cancers, as in our patient’s case, are exceedingly rare.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2090-6463
2090-6471
Relation: https://doaj.org/toc/2090-6463; https://doaj.org/toc/2090-6471
DOI: 10.1155/2016/7137691
URL الوصول: https://doaj.org/article/44ad1445cd674f2cbe332670ec5de2dd
رقم الأكسشن: edsdoj.44ad1445cd674f2cbe332670ec5de2dd
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20906463
20906471
DOI:10.1155/2016/7137691