Total: 5 |
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PMID (PMCID) | ||
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30906603 |
OTHER | |
Castleman Disease in a Patient with Common Variable Immunodeficiency. | ||
Ricciardi L, Furci F, Ieni A, Macri A. Case Reports Immunol. 2019;2019:5476383. |
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Castleman disease (CD) is a systemic disease clinically characterized by diffuse lymphadenopathy, splenomegaly, anemia, and systemic inflammatory symptoms. | ||
26387507 |
FEMALE | |
Anemia and autoimmunity markers in an adolescent with Castleman disease. | ||
Fretzayas A, Stasinopoulou A, Moustaki M, Stefos E, Kaniouras G, Nicolaidou P. Pediatr Int. 2015;57(6):1199-201. |
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This case emphasizes the need to investigate thoroughly for the underlying cause of anemia of inflammation and to include Castleman disease in the differential diagnosis, on the measurement of IL-6. | ||
26387507 |
FEMALE | |
Anemia and autoimmunity markers in an adolescent with Castleman disease. | ||
Fretzayas A, Stasinopoulou A, Moustaki M, Stefos E, Kaniouras G, Nicolaidou P. Pediatr Int. 2015;57(6):1199-201. |
||
Anemia and autoimmunity markers in an adolescent with Castleman disease. | ||
24367988 |
FEMALE | Child |
Iron-refractory microcytic anemia as the presenting feature of unicentric Castleman disease in children. | ||
Chandrakasan S, Bakeer N, Mo JQ, Cost C, Quinn CT. J Pediatr. 2014;164(4):928-30. |
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Surgical resection cured the anemia and the Castleman disease. | ||
24367988 |
FEMALE | Child |
Iron-refractory microcytic anemia as the presenting feature of unicentric Castleman disease in children. | ||
Chandrakasan S, Bakeer N, Mo JQ, Cost C, Quinn CT. J Pediatr. 2014;164(4):928-30. |
||
A diagnostic clue to Castleman disease is an elevated concentration of interleukin-6 in blood, which causes anemia by inducing the expression of the iron-regulatory hormone hepcidin. |