A Case of Ketron-Goodman DiseaseCarlesimo M.a · Tammaro A.a · Cox C.b · Mari E.a · Fidanza L.a · Narcisi A.a · Cacchi C.c · Camplone G.a
aU.O.C. Dermatology, bU.O.C. Hematology, and cUnit of Histopathology, II School of Medicine University of Rome ‘Sapienza’, Rome, Italy Corresponding Author
Alessandra Narcisi, MD
U.O.C. Dermatology, II School of Medicine University of Rome ‘Sapienza’
Via di Grottarossa, 1039, IT–00189 Rome (Italy)
Tel. +39 06 3377 5822, Fax +39 06 3377 5081, E-Mail email@example.com
Pagetoid reticulosis (PR) is a rare form of cutaneous T-cell lymphoma [Mod Pathol 2000;13:502–510]. Two variants of the disease are described: the localized type Woringer-Kolopp disease (WKD) and the disseminated type Ketron-Goodman disease (KGD). KGD may have disseminated lesions, high rate of recurrence and a guarded prognosis [Mod Pathol 2000;13:502–510]. In patients with KGD, therefore, long-term observation is necessary. Disappearance of cutaneous lesions does not mean resolution of the disease [J Am Acad Dermatol 2002;47:183–186]. Herein we report the case of an 84-year-old man with erythematous patches of the trunk and the upper and lower extremities in whom the diagnosis of KGD was made. We describe this case for the rarity of this pathology and for the good response to therapy (IFN).
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