Systemic lupus erythematosus


Hemolytic anemia

A type of anemia caused by premature destruction of red blood cells (hemolysis).


Total: 21

                       


(per page)
PMID (PMCID)
30568122
 MALE
IgM-mediated Warm Autoimmune Hemolytic Anemia: An Autopsy Report.
Ito T, Tojo N, Takashiro K, Yoshimura K, Yamamoto K, Hara S, Takesue K, Yoshimatsu N, Obata T, Takahara N.
Intern Med. 2019;58(7):999-1002.
A 79-year-old man with Sjogren's syndrome and systemic lupus erythematosus developed acute impaired consciousness and hemolytic anemia.
28515936
(5423708)
 OTHER
Pulse dose steroids in severe pulmonary arterial hypertension secondary to systemic lupus erythematosus.
Lee C, Elwing J.
SAGE Open Med Case Rep. 2017;5:2050313X17707153.
Because of coexisting systemic lupus erythematosus with hemolytic anemia and worsening pulmonary arterial hypertension, intensive immunosuppressive therapy with pulse dose steroids was initiated.
25716420
 FEMALE Adult
SLE presenting as multiple hemorrhagic complications.
Abdulla MC, Alungal J, Hashim S, Ali MM, Musambil M.
Lupus. 2015;24(10):1103-6.
On diagnostic evaluation she was found to have hemolytic anemia, thrombocytopenia and bilateral adrenal, subdural, soft tissue (scalp and orbit) hemorrhages due to systemic lupus erythematosus (SLE).
22644892
 FEMALE
Thrombotic thrombocytopenic purpura precipitated by thyrotoxicosis.
Chhabra S, Tenorio G.
J Clin Apher. 2012;27(5):265-6.
Thrombotic thrombocytopenic purpura (TTP) may be seen in association with autoimmune disorders such as immune hemolytic anemia and systemic lupus erythematosus, but rarely has it been associated with Graves' disease.
19789875
 FEMALE Adult
Systemic lupus erythematosus associated with vasculitic syndrome (Takayasu's arteritis).
Sachetto Z, Fernandes SR, Del Rio AP, Coimbra IB, Bertolo MB, Costallat LT.
Rheumatol Int. 2010;30(12):1669-72.
Two years later she presented malar rash, photosensitivity, nephropathy, leukopenia, lymphopenia and hemolytic anemia confirming the systemic lupus erythematosus (SLE) diagnosis.
19034453
 MALE Child
Chronic recurrent multifocal osteomyelitis in a patient with selective immunoglobulin M deficiency.
Makay B, Unsal E, Anal O, Gunes D, Men S, Cakmakci H, Ozer E.
Rheumatol Int. 2009;29(7):811-5.
Selective immunoglobulin M (IgM) deficiency is a rare primary immunodeficiency disease, which can be associated with autoimmune diseases such as systemic lupus erythematosus, Hashimoto's disease, or hemolytic anemia.
18483142
 MALE
Determination of hemolytic anemia through the study of (51)Cr red cell survival and splenic sequestration.
Willett AB, Grantham VV.
J Nucl Med Technol. 2008;36(2):95-8.
This procedure review presents a dual survival and sequestration study positive for hemolytic anemia and hypersplenism in an 83-y-old man with systemic lupus erythematosus.
17538567
 FEMALE Adult
Thrombotic microangiopathic hemolytic anemia in a patient with SLE: diagnostic difficulties.
Shah AA, Higgins JP, Chakravarty EF.
Nat Clin Pract Rheumatol. 2007;3(6):357-62.
A 19-year-old woman with newly diagnosed systemic lupus erythematosus (SLE) presented with hemolytic anemia, thrombocytopenia, hypertension, tonic-clonic seizures, blurry vision, nephrotic syndrome and renal insufficiency.
16038113
 FEMALE Middle Aged
Systemic lupus erythematosus with refractory hemolytic anemia effectively treated with cyclosporin A: a case report.
Wang SW, Cheng TT.
Lupus. 2005;14(6):483-5.
A 51 year old woman with systemic lupus erythematosus (SLE) serially developed thrombocytopenia, arthritis, lupus nephritis, pleuritis, mesenteric vasculitis and refractory hemolytic anemia during the past 19 years prior to presentation.
14635405
 FEMALE Middle Aged
[Successful treatment of intravenous cyclophosphamide pulse therapy for systemic lupus erythematosus complicated with steroid-resistant hemolytic anemia].
Tokunaga M, Saito K, Nakatsuka K, Nakayamada S, Nakano K, Tsujimura S, Ota T, Tanaka Y.
Nihon Rinsho Meneki Gakkai Kaishi. 2003;26(5):304-9.
[Successful treatment of intravenous cyclophosphamide pulse therapy for systemic lupus erythematosus complicated with steroid-resistant hemolytic anemia].
14635405
 FEMALE Middle Aged
[Successful treatment of intravenous cyclophosphamide pulse therapy for systemic lupus erythematosus complicated with steroid-resistant hemolytic anemia].
Tokunaga M, Saito K, Nakatsuka K, Nakayamada S, Nakano K, Tsujimura S, Ota T, Tanaka Y.
Nihon Rinsho Meneki Gakkai Kaishi. 2003;26(5):304-9.
Nephropathy, hemolytic anemia (Hb 6.3 g/dl and direct Coombs 3+) and high titers of antinuclear antibodies and anti-ds-DNA antibody were disclosed and she was diagnosed as systemic lupus erythematosus (SLE).
8970061
 MIXED_SAMPLE Adult
Cardiac valvular disease in scleroderma and systemic lupus erythematosus/scleroderma overlap associated with antiphospholipid antibodies.
Penmetcha M, Rosenbush SW, Harris CA.
J Rheumatol. 1996;23(12):2171-4.
We describe 2 cases with positive antiphospholipid antibodies (aPL); one with limited scleroderma associated with aortic valve vegetation, the 2nd with systemic lupus erythematosus/scleroderma overlap with recurrent venous thrombosis, pulmonary emboli, hemolytic anemia, and severe mitral regurgitation requiring valve replacement.
7791180
 FEMALE Child
Fatal myocardial infarction in an 8-year-old girl with systemic lupus erythematosus, Raynaud's phenomenon, and secondary antiphospholipid antibody syndrome.
Miller DJ, Maisch SA, Perez MD, Kearney DL, Feltes TF.
J Rheumatol. 1995;22(4):768-73.
An 8-year-old black girl with a 5 month history of systemic lupus erythematosus (SLE) and secondary antiphospholipid syndrome (APS) developed Raynaud's phenomenon, marked hemolytic anemia, and a fatal myocardial infarction (MI).
7899874
 FEMALE Adult
Thrombotic microangiographic hemolytic anemia in systemic lupus erythematosus.
Nesher G, Hanna VE, Moore TL, Hersh M, Osborn TG.
Semin Arthritis Rheum. 1994;24(3):165-72.
Thrombotic microangiographic hemolytic anemia in systemic lupus erythematosus.
8484132
 MALE Adult
Hypogammaglobulinemia and rheumatic disease.
Lee AH, Levinson AI, Schumacher HR Jr.
Semin Arthritis Rheum. 1993;22(4):252-64.
Autoimmune disorders such as immune thrombocytopenic purpura, immune hemolytic anemia, juvenile rheumatoid arthritis, systemic lupus erythematosus, dermatomyositis, Sjogren's syndrome, essential mixed cryoglobulinemia, chronic active hepatitis, and sarcoidosis have been reported in hypogammaglobulinemic patients.
8515607
 FEMALE Middle Aged
[A case of acute pulmonary hemorrhage and positive anti-glomerular basement membrane antibody in systemic lupus erythematosus].
Yamazaki K, Fujita J, Doi I, Abe S, Kawakami Y, Fukazawa Y.
Nihon Kyobu Shikkan Gakkai Zasshi. 1993;31(2):251-6.
She was diagnosed as having systemic lupus erythematosus (SLE) with positive anti-nuclear antibody, positive anti-DNA antibody, biologically false positive Wassermann reaction, auto-immune hemolytic anemia and photosensitive dermatoses.
1795445
 FEMALE
[An elderly case of systemic lupus erythematosus associated with herpes zoster, anemia, and hemiparesis].
Hashizume K, Sato M, Saeki S, Takamoto S, Mino Y, Onishi T.
Nihon Ronen Igakkai Zasshi. 1991;28(6):817-22.
An elderly case of systemic lupus erythematosus (SLE) with suspected hemolytic anemia was experienced.
1689774
 MIXED_SAMPLE Adult
Manifestations and treatment of human parvovirus B19 infection in immunocompromised patients.
Koch WC, Massey G, Russell CE, Adler SP.
J Pediatr. 1990;116(3):355-9.
In a 19-year-old patient with systemic lupus erythematosus and hemolytic anemia, an aplastic crisis lasted 2 weeks.
2746588
 MIXED_SAMPLE Adult
Primary antiphospholipid syndrome.
Alarcon-Segovia D, Sanchez-Guerrero J.
J Rheumatol. 1989;16(4):482-8.
An antiphospholipid antibody (APLA) syndrome has been proposed for those patients with systemic lupus erythematosus (SLE) or with other connective tissue diseases who have APLA and manifestations that seem related to their effect (venous thrombosis, arterial occlusions, thrombocytopenia, hemolytic anemia, recurrent fetal loss, leg ulcers, and livedo reticularis).
3963988
 FEMALE Adult
Canada-Cronkhite syndrome associated with systemic lupus erythematosus.
Kubo T, Hirose S, Aoki S, Kaji T, Kitagawa M.
Arch Intern Med. 1986;146(5):995-6.
The exacerbation of systemic lupus erythematosus, presenting with hemolytic anemia and subsequently with profound proteinuria, was seen during the course of this syndrome.