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2013, Number 4

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Med Cutan Iber Lat Am 2013; 41 (4)

Cutaneous plasmacytosis

Bernat GJ, Prats A, Barbera E, Marti ME, Marquina A
Full text How to cite this article

Language: Spanish
References: 8
Page: 176-178
PDF size: 678.54 Kb.


Key words:

cutaneous plasmacytosis, systemic plasmacytosis, plasma cells, polyclonal hypergammaglobulinaemia.

ABSTRACT

Cutaneous plasmacytosis is a rare disorder characterized by a benign proliferation of mature plasma cells that appears as multiple red to dark brown skin lesions, often associated with polyclonal hypergammaglobulinaemia. We report the case of a 33-year-old white woman who presented with reddish brown plaques restricted to trunk and scalp. Histologically, the lesions showed a moderately dense superficial and deep perivascular and periadnexal infiltrate composed predominantly of mature plasma cells without atypia.


REFERENCES

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  2. Kimura K, Fujita H, Ishihama S. A case of cutaneous plasmacytosis. Hihu Rinsho 1983; 25: 1045-50.

  3. Watanabe S, Ohara K, Kukita A, Mori S. Systemic plasmacytosis. A syndrome of peculiar multiple skin eruptions, generalized lymphadenopathy, and polyclonal hypergammaglobulinemia. Arch Dermatol 1986; 122: 1314-20.

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  6. González-López MA; González-Vela MC; Blanco R, Fernández-Llaca H, Val-Bernal JF. Cutaneous plasmacytosis limited to the extemities in a white patient: an unusual clinical picture. Cutis 2010; 86: 143-7.

  7. López-Estebaranz JL, Rodríguez-Peralto JL, Ortiz Romero L, Vanaclocha F, Iglesias Díez L. Cutaneous plasmacytosis: report of a case in a white man. J Am Acad Dermatol 1994; 31: 897-900.

  8. Uhara H, Saida T, Ikegawa S, Yamazaki Y, Mokoshiba H, Nijoh S, et al. Primary cutaneous plasmacytosis: report of three cases and review of the literature. Dermatology 1994; 189: 251-5.




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C?MO CITAR (Vancouver)

Med Cutan Iber Lat Am. 2013;41