A Case of Ketron-Goodman Disease.

A Case of Ketron-Goodman Disease.
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DOI:
10.1159/000236057
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发表时间:
2009-09-12
影响因子:
0.9
通讯作者:
Camplone G
Camplone G
中科院分区:
其他
文献类型:
--
作者:
Carlesimo M;Tammaro A;Cox C;Mari E;Fidanza L;Narcisi A;Cacchi C;Camplone G

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page - toid reticulosis (PR)是一种罕见的皮肤t细胞淋巴瘤[现代病理杂志,2000;13:50 - 51]。该疾病有两种变体:局部型Woringer-Kolopp病(WKD)和弥散型Ketron-Goodman病(KGD)。KGD可能具有弥散性病变,复发率高,预后谨慎[现代病理杂志2000;13:502-510]。因此,对于KGD患者,长期观察是必要的。皮肤病变消失不等于疾病的消退[J]; journal of clinical nursing; 2002; 17(1): 184 - 184。在这里,我们报告的情况下,84岁的男子与红斑斑块的躯干和上肢和下肢在谁的诊断KGD作出。我们描述这个病例罕见的病理和良好的反应治疗(IFN)。
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).
DOI: 10.1056/nejm198801213180307
发表时间: 1988-01-21
影响因子: 158.5
作者:
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