-transparent.png){kind=logo}
Sézary syndrome is a form of leukemia-lymphoma characterized clinically by erythroderma, pruritus, adenopathy, and circulating atypical cells with cerebriform nuclei. Histologically, atypical lymphocytes in the dermis and Pautrier's microabscesses are often present in skin biopsy specimens. We herein report a typical case of Sézary syndrome showing T-suppressor-cell characteristics, and related literatures are reviewed.
Related Publications
C C Chen, and
W J Wang, and
W L Hwang, and
G Chou
July 1976,
The British journal of dermatology,
C C Chen, and
W J Wang, and
W L Hwang, and
G Chou
April 1975,
Medizinische Monatsschrift,
C C Chen, and
W J Wang, and
W L Hwang, and
G Chou
May 1976,
Nihon rinsho. Japanese journal of clinical medicine,
C C Chen, and
W J Wang, and
W L Hwang, and
G Chou
January 1998,
Ryoikibetsu shokogun shirizu,
C C Chen, and
W J Wang, and
W L Hwang, and
G Chou
November 1977,
International journal of dermatology,
C C Chen, and
W J Wang, and
W L Hwang, and
G Chou
January 1983,
Acta medica portuguesa,
C C Chen, and
W J Wang, and
W L Hwang, and
G Chou
June 2014,
Surgical pathology clinics,
C C Chen, and
W J Wang, and
W L Hwang, and
G Chou
January 1980,
Actas dermo-sifiliograficas,
