2011
DOI: 10.1111/j.1442-200x.2011.03369.x
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Six‐year‐old girl with primary cutaneous aggressive epidermotropic CD8+ T‐cell lymphoma

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Cited by 19 publications
(13 citation statements)
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“…Apart from this case, Kikuchi et al . documented primary cutaneous aggressive epidermotropic CD8 + T‐cell lymphoma in a 6‐year‐old girl, presenting with unusual features including hypersensitivity to mosquito bites, peripheral lymph node involvement by CD8+ cells and large (up to 10 cm) cutaneous necrotic lesions …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Apart from this case, Kikuchi et al . documented primary cutaneous aggressive epidermotropic CD8 + T‐cell lymphoma in a 6‐year‐old girl, presenting with unusual features including hypersensitivity to mosquito bites, peripheral lymph node involvement by CD8+ cells and large (up to 10 cm) cutaneous necrotic lesions …”
Section: Resultsmentioning
confidence: 99%
“…104 Apart from this case, Kikuchi et al documented primary cutaneous aggressive epidermotropic CD8 + T-cell lymphoma in a 6-year-old girl, presenting with unusual features including hypersensitivity to mosquito bites, peripheral lymph node involvement by CD8+ cells and large (up to 10 cm) cutaneous necrotic lesions. 105 Primary cutaneous c/d+ T-cell lymphoma (CGD-TCL) is a rare malignancy characterized by a clonal proliferation of mature activated c/d T cells thought to derive from local organ-specific c/d T-cell populations. 106,107 The disease is rare with approximately 100 cases reported to date.…”
Section: Extranodal Nk/t-cell Lymphoma Nasal-type Hydroa Vacciniformentioning
confidence: 99%
“…Recently, Cerroni et al reported subcutaneous panniculitis‐like T‐cell lymphoma with features similar to those of lupus panniculitis; however, the involvement of the epidermis was not evident in these cases . Our case should also not be confused with primary cutaneous aggressive epidermotropic CD8 + T‐cell lymphoma, which has been reported in children . However, primary cutaneous aggressive epidermotropic CD8 + T‐cell lymphoma is usually aggressive in its clinical behavior, whereas our patient was living for 3 years with the disease and responded well to prednisone.…”
Section: Discussionmentioning
confidence: 45%
“…10,11 Our case should also not be confused with primary cutaneous aggressive epidermotropic CD8 + T-cell lymphoma, which has been reported in children. 12 However, primary cutaneous aggressive epidermotropic CD8 + T-cell lymphoma is usually aggressive in its clinical behavior, whereas our patient was living for 3 years with the disease and responded well to prednisone. Histopathologically, primary cutaneous aggressive epidermotropic CD8 + T-cell lymphoma usually occur in the epidermis and dermis, 5 -7 whereas our case prominently involved the subcutaneous tissue.…”
Section: Discussionmentioning
confidence: 58%
“…To date, there is no controlled trial showing a survival benefit from any of the therapies. In the future, reduced-intensity conditioning followed by allogeneic stem cell transplantation may be effective as an alternative treatment 14 , even among pediatric patients. With progression of the primary CL, other clinical features such as fever, wasting, lymphadenopathy, hepatosplenomegaly and loss of mobility are often observed.…”
Section: Discussionmentioning
confidence: 99%