Two cases of pseudolymphoma on the lips
Two cases of pseudolymphoma on the lips
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嘴唇假性淋巴瘤二例
DOI:
10.1111/bjd.12837
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发表时间:
2014
影响因子:
10.3
通讯作者:
Shimizu H
中科院分区:
文献类型:
--
作者:
Haga N;Nishie W;Hata H;Miyauchi T;Muramatsu K;Kitamura S;Osawa R;Shimizu H
Patient 2, a 42-year-old Japanese female with a 5-year-history of asymptomatic papules on the lips, presented at our hospital. Initially, the skin eruptions waxed and waned, but for the 4 months prior to the initial visit, they had been persistent (Fig. 2a). Like patient 1, she had no causative history, but dental metal was noticed (Fig. 2a). Histopathology from a lesion showed diffuse infiltrates of mononuclear cells without atypia, which formed lymphoid follicle-like structures (Fig. 2b), and the immunological properties for CD3, CD10, CD20, CD30, Bcl-6 and HSV-I were similar to those of patient 1 (Fig. 2b). EBER in situ hybridization showed no positive cells (not shown). Immunoglobulin j and k light chain-restricted cell populations were not observed, and polymerase chain reaction targeting the joining region of the immunoglobulin heavy chain gene2 excluded monoclonal proliferation (not shown). Laboratory investigation showed increased eosinophils (9Á0%; normal: 0–6Á0%) and positivity for antinuclear antibodies (9 160), but serum interleukin-2-receptor level was within the normal limit. We diagnosed the skin lesions as B-cell pseudolymphoma. The patient did not wish to receive
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影响因子:
--
作者:
J. Pablos;P. Carreira;L. Morillas;G. Montalvo;C. Ballestín;J. Gómez
通讯作者:
J. Gómez
影响因子:
3.4
作者:
J. Shin;S. Seo;Byoung;Il;S. Son
通讯作者:
S. Son
DOI:
10.1016/j.bjoms.2004.02.026
发表时间:
2005
期刊:
The British journal of oral & maxillofacial surgery
影响因子:
--
作者:
Yuk;Yee‐Hsiung Shen;Cheng‐Chung Lin;Li
通讯作者:
Li
影响因子:
5.5
作者:
Hiromi Komatsu;S. Aiba;S. Mori;Katsuhiko Suzuki;Hachiro Tagami
通讯作者:
Hachiro Tagami