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| PubMed | |
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Article by Hui,y |
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Article by Zheng,B.J |
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Article by Chen,g |
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Article by Yu,Q.Q |
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Article by Zhang,G.Y |
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��ժҪ�� �����У�9�꣬��ȫ�����ŧ�塢���衢����8������Ƥ����֯�����������黯�����ܰ����������C�ͣ����ܰ������������ԭ����Ƥ��CD30+�ܰ������Լ��������������ԣ������о����٣���֯����ѧ�ɷ�ΪA��B��C���͡��ٴ���������Ϊ���Զ�����̦�����C����֯����ѧ��ԭ����Ƥ��CD30+����Դ�ϸ�����ܰ������ƣ��ʼ��������Ϊ��Ҫ�� ���ؼ��ʡ� �ܰ���������� ��ͯ
Lymphomatoid papulosis type C in a child
HUI Yun, ZHENG Bing-jie, CHEN Hao, WANG Qian-qiu, ZHANG Guo-yi. Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing 210042, China Corresponding author: ZHANG Guo-yi, Email: zhangguoyi1010@sina.com ��Abstract�� A 9-year-old boy was admitted to the hospital for recurrent papules, pustules, crust and necrosis all over the body for 8 years. A diagnosis of lymphomatoid papulosis type C was made according to histopathological and immunohistochemical findings. Lymphomatoid papulosis, as a kind of self-healing primary cutaneous CD30+ lymphoproliferative disorder, can be histopathologically divided into 3 types, i.e., A, B and C, and little is known about its pathogenesis. Lymphomatoid papulosis is often misdiagnosed as pityriasis lichenoides et varioliformis acuta. Lymphomatoid papulosis type C should be pathologically differentiated from primary cutaneous CD30+ anaplastic large cell lymphoma. ��Key words�� Lymphomatoid papulosis; Child