Total: 4 |
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PMID (PMCID) | ||
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22172955 |
MALE | Adult |
Cutaneous and systemic plasmacytosis showing histopathologic features as mixed-type Castleman disease: a case report. | ||
Chen H, Xue Y, Jiang Y, Zeng X, Sun JF. Am J Dermatopathol. 2012;34(5):553-6. |
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Cutaneous and systemic plasmacytosis showing histopathologic features as mixed-type Castleman disease: a case report. | ||
21940235 |
MALE | Middle Aged |
Cutaneous and systemic plasmacytosis vs. cutaneous plasmacytic castleman disease: review and speculations about pathogenesis. | ||
Haque M, Hou JS, Hisamichi K, Tamada K, Cusack CA, Abdelmalek M, Brown RE, Vonderheid EC. Clin Lymphoma Myeloma Leuk. 2011;11(6):453-61. |
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Cutaneous and systemic plasmacytosis (C/SP), human herpes virus-8 (HHV8), negative multicentric plasmacytic Castleman disease (MPCD), and idiopathic plasmacytic lymphadenopathy are polyclonal plasma cell proliferations of unknown etiology that predominantly affect Asian individuals. | ||
18573783 |
MALE | Middle Aged |
Lymphoplasmacytic infiltrate of regional lymph nodes in Kuttner's tumor (chronic sclerosing sialadenitis): a report of 3 cases. | ||
Kojima M, Miyawaki S, Takada S, Kashiwabara K, Igarashi T, Nakamura S. Int J Surg Pathol. 2008;16(3):263-8. |
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The present 3 cases indicated that regional lymph node of Kuttner's tumor may show reactive follicular hyperplasia and prominent interfollicular plasmacytosis and should be differentiated from various benign and malignant lymphoproliferative disorders including systemic rheumatic disease, plasma cell type of Castleman disease, and lymph node involvement of marginal B-cell lymphoma of the mucosa-associated lymphoid tissue type showing prominent plasma cell differentiation. | ||
16860182 |
MALE | Middle Aged |
Renal involvement in multicentric Castleman disease with glomeruloid hemangioma of skin and plasmacytoma. | ||
Uthup S, Balachandran K, Ammal VA, Abdul Salam R, George J, Nair GM, Leela M. Am J Kidney Dis. 2006;48(2):e17-24. |
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Axillary lymph node biopsy showed findings consistent with Castleman disease of the hyaline vascular type associated with interfollicular plasmacytosis. |