Two cases with pulmonary crises with sickle cell anemia were presented with up to date knowledge.
📌 3 Key Takeaways
🎯
Objective & Hypothesis:Sickle cell anemia is a chronic hemolytic anemia with vasoocclusive crisis and is the most common symptomatic event that causes tissue hypoxia in many systems.
📊
Key Findings & Data:Pulmonary crisis is one of them and its the major cause of mortality and morbidity in sickle cell anemia.
💡
Conclusion & Impact:Two cases with pulmonary crises with sickle cell anemia were presented with up to date knowledge.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Sickle cell anemia is a chronic hemolytic anemia with vasoocclusive crisis and is the most common symptomatic event that causes tissue hypoxia in many systems. Pulmonary crisis is one of them and its the major cause of mortality and morbidity in sickle cell anemia. Furthermore, pulmonary crisis is the second clinical situation for hospitalization. Pneumoia must be thought in differential diagnosis and is too difficult to rule out. Two cases with pulmonary crises with sickle cell anemia were presented with up to date knowledge.
🔖
Cite This Article
ŞAŞMAZ, İ., KILINÇ, Y., BİRBİÇER, H., KİBAR, M., LEBLEBİSATAN, G., ARIBOĞAN, A., ANTMEN, B. (2022). Pulmonary crisis in sickle cell anemia. Göztepe Tıp Dergisi, Cilt: 20 - Sayı: 2, 108–110. https://ajindex.com/articles/526388
Herrick JB: Peculiar elongated and sickle shaped reci corpusculs in a case of severe anemia. Arch Intern Med 6:517, 1910
Wang WC: Sickle celi anemia and olher sickling syndromes. ln:Greer JP, Foerster J, Lukens JN, Rodgers GM, Paraskevas F, Glader B eds. Winlrobe's Clinical Hematology Second ed. Philadelphia, Lippincott Williams and Wilkins, 1263-1312, 2004
Dover GJ, Platt OS: Sickle cell disease In: Nathan DG, Orkin SH, Ginsburg D, Look TA eds. Hematology of infancy and childhood. 6lh ed, Philadelphia, WB Saunders Company, 790-841, 2003
Caslro O, Brambilla DJ, Thurington B, et ah The acute chest syndrom in sickle cell disease:incidence and rise factors. The cooperative study in sickle cell disease. Blood 84:643-649, 1994
Kılınç Y: Orak hücre anemisinin tedavisi. Arcasaoy A, Canatan D, Köse MR, Üstündağ M, editörler. Talasemi ve Hemoglobinopati Önlem-Tanı-Tedavi Kitabı, Sağlık Bakanlığı Yayınlan i 17-125, 2003
Siddiqui AK, Ahmed S: Pulmonary man is fes ta ti ons of sickle cell disease. Postgrad Med 79:384-390, 2003
Kılınç Y, Kiimi M, Yılmaz B, Tanyeli A: Zinc and copper values in serum and erythrocytes in sickle cell homozygous and trait children. Ada Pediatr Scand 80:873-874
Alouch JR, Kılınç Y, Aksoy M, et al: Sickle ceil anemia among Eti-Türks:hemalological, clinical and genetic observations. Br J Hematol 6-1:45-49, 1986, 9. Kılınç Y, Aktnanlar N, Kümi M, et al: The incidences of hemoglobinopathies and thalassemias in cord bloodof newborns from Çukurova Province. Med Bull 25:9-14, 1992
Kılınç Y: Osmaniye merkez ve çevresi ilkokul ve ortaöğrenim öğrencilerinde hemoglobinopati, talassemia ve G-6-PD eksikliği araştırması. Tarih içinde bütün yönleriyle Osmaniye i. Simpozyum Kitabı. 15-17 Kasttrı 1993, 145-50
Feldman L, Gross R, Garon J, et al: Sickle cell patient with an acute chest syndrome and a negative x-ray:Potential role of the ventilation and perfusion (V/Q) lung scan. Am J Hematol 74:214-215, 2003
Lombardo T, Rosso R, La Ferla A, et al: Acute chest syndrome:the role of erythro-exchange in patients with sickle cell disease in Sicily. Transfus Apheresis Sci 29:39-44, 2003
Danielson CF: The role of red blood cell Exchange transfusion in the treatment and prevention of complications of sickle cell disease. Ther Apher 6:24-31, 2002