1.A Case of Cutaneous T Cell Lymphoma Presenting as Papuloerythroderma of Ofuji.
Jung Im NA ; Hee Jin BYUN ; Kwang Hyun CHO
Korean Journal of Dermatology 2007;45(4):373-377
Papuloerythroderma of Ofuji (PEO) is an uncommon entity of unknown etiology, characterized by coalescing erythematous papules sparing skin folds. A number of cases have described the association of this disorder with malignant with pathology, mainly with cutaneous T cell lymphoma. Such reports give rise to the suggestion that PEO may be a precursor of lymphoma or a form of cutaneous T cell lymphoma. We report a case of PEO, which was diagnosed as cutaneous T-cell lymphoma only 2 months after the development of skin lesions, and rapidly progressed. This case suggests the presence of a variant of cutaneous T cell lymphoma with clinical feature of PEO, which is different from mycosis fungoides or S zary syndrome.
Lymphoma
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Lymphoma, T-Cell, Cutaneous*
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Lymphoma, T-Cell, Peripheral
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Mycosis Fungoides
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Pathology
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Skin
3."Myositis-like" T-cell lymphoma: report of a case.
Xiao-ge ZHOU ; Yan SHI ; Gang CHEN ; Yuan-yuan ZHENG ; Yan-ning ZHANG ; Shu-hong ZHANG
Chinese Journal of Pathology 2008;37(6):422-423
4.Subcutaneous panniculitis-like T-cell lymphoma in a case.
Chinese Journal of Pediatrics 2008;46(7):512-512
8.Analysis of mature T-cell and NK-cell lymphoma with CD30 expression based on latest WHO classification.
Yanfen FENG ; ; Jia FU ; ; Shumei YAN ; ; Yihong LING ; ; Yili HUANG ; ; Muyan CAI ; ; Huilan RAO ;
Chinese Journal of Pathology 2014;43(8):508-511
OBJECTIVETo investigate the frequency of different types of mature T- and NK-cell lymphomas diagnosed in a 4-year period at Sun Yat-sen University Cancer Center, and to study baseline CD30 for potential anti-CD30 targeted therapy in mature T- and NK-cell lymphoma.
METHODSAll cases of mature T- and NK-cell lymphoma diagnosed at Sun Yat-sen University Cancer Center from September 1, 2009 to August 31, 2013, were reviewed. Paraffin-blocks of available 164 consecutive cases were stained for CD30 immunohistochemistry using EnVision protocol.
RESULTSA total of 625 cases of mature T- and NK-cell lymphomas were diagnosed and the most common type was extranodal NK/T cell lymphoma (ENKTL), nasal type 319 (51.0%) cases, followed by angioimmunoblastic T-cell lymphoma (AITL) (119 cases, 19.0%), peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS) (81 cases, 13.0%), and anaplastic large-cell lymphoma (ALCL), including 48 cases (7.7%) of systematic ALCL and 11 cases (1.8%) of primary cutaneous ALCL. Besides ALCL, ENKTL had the highest expression rate of CD30 among the 164 cases, with positivity observed in 41 cases (62.1%, 41/66). Only 1 case of PTCL-NOS was CD30 positive. CD30 was not expressed in all 28 cases of AITL and other rare types of mature T- and NK-cell lymphoma.
CONCLUSIONSThe frequency of different types of mature T- and NK-cell lymphoma encountered at Sun Yat-sen University Cancer Center was similar to that seen in other areas of China and other Asia countries. CD30 expression is different among several types of mature T- and NK-cell lymphoma. In addition to ALCL, ENKTL has the highest expression rate of CD30, which may be a candidate disease for anti-CD30 targeted therapy.
China ; epidemiology ; Humans ; Immunohistochemistry ; Killer Cells, Natural ; Lymphoma, Extranodal NK-T-Cell ; epidemiology ; pathology ; Lymphoma, Large-Cell, Anaplastic ; epidemiology ; pathology ; Lymphoma, Primary Cutaneous Anaplastic Large Cell ; epidemiology ; pathology ; Lymphoma, T-Cell, Peripheral ; epidemiology ; pathology ; T-Lymphocytes
9.Histologic evaluation of malignant lymphoma.
Chinese Journal of Pathology 2011;40(4):217-219
Dendritic Cells, Follicular
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pathology
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Diagnosis, Differential
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Humans
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Leukemia, Lymphocytic, Chronic, B-Cell
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pathology
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Lymphoma
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pathology
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Lymphoma, Extranodal NK-T-Cell
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pathology
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Lymphoma, Follicular
;
pathology
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Lymphoma, Large B-Cell, Diffuse
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pathology
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Lymphoma, Large-Cell, Anaplastic
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pathology
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Lymphoma, Mantle-Cell
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pathology
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Lymphoma, T-Cell, Peripheral
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pathology
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Neoplasm Invasiveness
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Precursor Cell Lymphoblastic Leukemia-Lymphoma
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pathology