A Rare Case of Cutaneous Plasmacytosis in a Korean Male

المؤلفون المشاركون

Georgesen, Corey
Kheterpal, Meenal
Pulitzer, Melissa

المصدر

Case Reports in Pathology

العدد

المجلد 2017، العدد 2017 (31 ديسمبر/كانون الأول 2017)، ص ص. 1-6، 6ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2017-08-07

دولة النشر

مصر

عدد الصفحات

6

التخصصات الرئيسية

الأمراض

الملخص EN

Cutaneous and systemic plasmacytosis are reactive disease processes that occur in middle-aged Japanese and Chinese men.

Systemic plasmacytosis, defined by plasmacytic infiltration of two organ systems, might rarely progress to lymphoma.

Cutaneous plasmacytosis, however, is chronic and benign and is characterized by the development of multiple plasma cell-rich infiltrates in the skin.

We present a case of cutaneous plasmacytosis in a 46-year-old Korean male.

The patient demonstrated classic features of the disease entity, including disseminated red-brown plaques, differentiated plasmacytoid infiltrates on biopsy, hypergammaglobulinemia, and the absence of systemic disease.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Georgesen, Corey& Kheterpal, Meenal& Pulitzer, Melissa. 2017. A Rare Case of Cutaneous Plasmacytosis in a Korean Male. Case Reports in Pathology،Vol. 2017, no. 2017, pp.1-6.
https://search.emarefa.net/detail/BIM-1148890

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Georgesen, Corey…[et al.]. A Rare Case of Cutaneous Plasmacytosis in a Korean Male. Case Reports in Pathology No. 2017 (2017), pp.1-6.
https://search.emarefa.net/detail/BIM-1148890

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Georgesen, Corey& Kheterpal, Meenal& Pulitzer, Melissa. A Rare Case of Cutaneous Plasmacytosis in a Korean Male. Case Reports in Pathology. 2017. Vol. 2017, no. 2017, pp.1-6.
https://search.emarefa.net/detail/BIM-1148890

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1148890