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Verfasst von:Toberer, Ferdinand [VerfasserIn]   i
 Hartschuh, Wolfgang [VerfasserIn]   i
 Hadaschik, Eva [VerfasserIn]   i
Titel:Primary cutaneous CD4+ small- to medium-sized pleomorphic T-cell lymphoma
Titelzusatz:temporary remission by oral doxycycline
Verf.angabe:Ferdinand Toberer, Wolfgang Hartschuh, Eva Hadaschik
E-Jahr:2013
Jahr:June 12, 2013
Umfang:4 S.
Fussnoten:Im Titel ist das "+"-Zeichen hochgestellt ; Gesehen am 07.02.2022
Titel Quelle:Enthalten in: JAMA dermatology
Ort Quelle:Chicago, Ill. : American Medical Association, 2013
Jahr Quelle:2013
Band/Heft Quelle:149(2013), 8, Seite 956-959
ISSN Quelle:2168-6084
Abstract:In the recent World Health Organization-European Organisation for Research and Treatment of Cancer classification, primary cutaneous CD4+ small- to medium-sized pleomorphic T-cell lymphoma is listed as a provisional entity that is histopathologically characterized by pleomorphic CD3+/CD4+/CD8−/CD30− T lymphocytes. Clinically, it is characterized by solitary tumors mostly affecting the head and neck area and by an indolent clinical course with an estimated 5-year survival of about 60% to 80%. Currently, therapeutic options include topical or systemic treatment with glucocorticoids, local excision of solitary lesions, radiotherapy, and chemotherapy (eg, cyclophosphamide) in cases of aggressive clinical behavior or systemic disease.We present the case of a 21-year-old female patient with a 5-year history of a solitary, slowly growing tumor of the right cheek. Histopathologic findings revealed a primary cutaneous CD4+ small- to medium-sized pleomorphic T-cell lymphoma with an admixture of numerous CD20+ B cells representing almost half of the infiltrate. In this patient we achieved a temporary (13 months) complete remission of the lymphoma by oral treatment with doxycycline monohydrate, 200 mg per day.Doxycycline is a relatively nontoxic and well-tolerated oral agent and should be considered as a therapeutic option in primary cutaneous CD4+ small- to medium-sized pleomorphic T-cell lymphoma, especially in cases with a high percentage of B lymphocytes and no signs of systemic disease.
DOI:doi:10.1001/jamadermatol.2013.4162
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1001/jamadermatol.2013.4162
 DOI: https://doi.org/10.1001/jamadermatol.2013.4162
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1788651677
Verknüpfungen:→ Zeitschrift

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