Primary Sjögren Syndrome Presenting with Hemolytic Anemia and Pure Red Cell Aplasia Following Delivery due to Coombs-negative Autoimmune Hemolytic Anemia and Hemophagocytosis

Author:

Komaru Yohei1,Higuchi Takakazu1,Koyamada Ryosuke1,Haji Youichiro2,Okada Masato2,Kamesaki Toyomi3,Okada Sadamu1

Affiliation:

1. Division of Hematology, St. Luke's International Hospital, Japan

2. Division of Allergy and Rheumatology, St. Luke's International Hospital, Japan

3. Center for Community Medicine, Jichi Medical University, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Reference20 articles.

1. 1. Ramakrishna R, Chaudhuri K, Sturgess A, Manoharan A. Haematological manifestations of primary Sjögren's syndrome: a clinicopathological study. Q J Med 84: 547-554, 1992.

2. 2. Zhou JG, Qing YF, Jiang L, Yang QB, Luo WF. Clinical analysis of primary Sjögren's syndrome complicating anemia. Clin Rheumatol 29: 525-529, 2010.

3. 3. Kamesaki T, Oyamada T, Omine M, Ozawa K, Kajii E. Cut-off value of red-blood-cell-bound IgG for the diagnosis of Coombs-negative autoimmune hemolytic anemia. Am J Hematol 84: 98-101, 2009.

4. 4. Baimpa E, Dahabreh IJ, Voulgarelis M, Moutsopoulos HM. Hematologic manifestations and predictors of lymphoma development in primary Sjögren syndrome: clinical and pathophysiologic aspects. Medicine 88: 284-293, 2009.

5. 5. Alexander EL, Arnett FC, Provost TT, Stevens MB. Sjögren's syndrome: association of anti-Ro(SS-A) antibodies with vasculitis, hematologic abnormalities, and serologic hyperreactivity. Ann Intern Med 98: 155-159, 1983.

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