Primary cutaneous peripheral T‐cell lymphoma, not otherwise specified, associated with lymphomatoid papulosis after a 9‐year follow up: A case report
Primary cutaneous peripheral T‐cell lymphoma, not otherwise specified, associated with lymphomatoid papulosis after a 9‐year follow up: A case report
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原发性皮肤外周 T 细胞淋巴瘤(未另有说明)9 年随访后与淋巴瘤样丘疹病相关:病例报告
DOI:
10.1111/1346-8138.15351
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发表时间:
2020
期刊:
影响因子:
--
通讯作者:
Jinnin Masatoshi
中科院分区:
文献类型:
--
作者:
Muraoka Kyoko;Fujimoto Masakazu;Iwahashi Yoshifumi;Matsuzaki Ibu;Yonei Nozomi;Murata Shin‐ichi;Jinnin Masatoshi
Lymphomatoid papulosis (LyP) is a self‐limiting cutaneous T‐cell lymphoproliferative disorder that may progress into malignant lymphoma. Most of the previously reported associated lymphomas are primary cutaneous anaplastic large‐cell lymphoma and mycosis fungoides with a low mortality rate. We report a case of primary cutaneous peripheral T‐cell lymphoma, not otherwise specified (pcPTCL‐NOS), associated with LyP after long‐term follow up. The patient was a 79‐year old Japanese man followed up for 9 years. He suddenly developed a 3‐cm ulcerated lesion on his forehead, which was diagnosed as an exacerbation of LyP. The lesion regressed after conservative treatment, but the patient soon developed multifocal pcPTCL‐NOS. Thereafter, the patient developed pneumonia and cerebral infarction and died within a few months of the onset of malignant lymphoma. Aggressive cutaneous lymphoma may develop in LyP patients. The present case re‐emphasizes the need for careful follow up of patients with persistent LyP.
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影响因子:
1.7
作者:
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通讯作者:
Y. Amoh
DOI:
10.1097/dad.0000000000000970
发表时间:
2017
期刊:
The American Journal of dermatopathology
影响因子:
--
作者:
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作者:
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Uzun S
DOI:
10.1097/pas.0000000000001256
发表时间:
2019
期刊:
The American Journal of Surgical Pathology
影响因子:
--
作者:
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通讯作者:
L. Cerroni
影响因子:
2
作者:
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通讯作者:
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