Manifestasi Klinis dan Manajemen Autoimmune Anemia Hemolytic (AIHA): Laporan Kasus Pada Pasien Perempuan Usia 40 Tahun

Authors

  • Jodi Setiawan Universitas Tarumanagara
  • Albert Tri Rustamadji Universitas Tarumanagara

Abstract

Autoimmune hemolytic anemia (AIHA) is decompensated acquired hemolysis caused by the body's immune system working against its own red blood cell antigens. A 40-year-old female patient came to the emergency room with complaints of black stools like tar, her eyes looked yellow, her body felt weak and she had a headache that had been felt for 5 days before she was admitted to hospital. The patient had a similar complaint which was felt approximately 4 years ago. On physical examination of the eyes, anemic conjunctiva and icteric sclera were found. On abdominal examination, grade 1-2 splenomegaly was found. Laboratory examination revealed a decrease in the number of erythrocytes, hemoglobin, hematocrit, platelets and an increase in the number of SGPT, SGOT, total bilirubin, direct bilirubin and indirect bilirubin. On examination of the peripheral blood images, mild anisocytosis, polychromasis and thrombocytopenia were found. Treatment for these patients is by using corticosteroids.

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Published

2024-11-03

How to Cite

Setiawan, J., & Rustamadji, A. T. (2024). Manifestasi Klinis dan Manajemen Autoimmune Anemia Hemolytic (AIHA): Laporan Kasus Pada Pasien Perempuan Usia 40 Tahun. Jurnal Ners, 9(1), 175–178. Retrieved from http://journal.universitaspahlawan.ac.id/index.php/ners/article/view/31239

Issue

Vol. 9 No. 1 (2025): November-Januari

Section

Articles

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Copyright (c) 2024 Jurnal Ners

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