scholarly journals Bone Marrow Necrosis and Fat Embolism in a Patient with Sickle Cell Crisis, a Fatal Complication

Author(s):  
Kaur Gagandeep ◽  
Olayinka Oluwaseyi ◽  
Gupta Gunjan
2014 ◽  
Vol 5 (2) ◽  
pp. 74-76 ◽  
Author(s):  
Laxmi P. Dhakal ◽  
Kirk Bourgeois ◽  
Kevin M. Barrett ◽  
William D. Freeman

2019 ◽  
Vol 77 (3) ◽  
pp. 318-322 ◽  
Author(s):  
Jérôme Debus ◽  
Bénédicte Dumont ◽  
Camille Le Breton ◽  
Malo Emery ◽  
Edith Peynaud-Debayle ◽  
...  

Blood ◽  
1982 ◽  
Vol 60 (6) ◽  
pp. 1411-1419 ◽  
Author(s):  
PF Milner ◽  
M Brown

Abstract Bone marrow infarction was investigated by 99mTc-sulfur colloid imaging in 42 patients with sickle cell anemia (SS) over a period of 2 yr. Marrow defects were demonstrated in 28 patients (66.6%), and in 15 (aged 19--52 yr), they were matched by roentgenographic evidence of medullary bone infarction. Repeated images showed no change in the size or site of these defects. Among 13 patients (aged 6--32 yr), all in crisis when initially examined, marrow defects were not associated with roentgenographic changes, and in many cases, repeated images showed resolution or decrease in size of the defects in 3--6 mo, even if the limb had been swollen and the marrow defect large. Among 14 patients (aged 18--36 yr), all asymptomatic at the time of study, no defects were found. Comparison of hematologic variables revealed a higher mean hemoglobin and hematocrit level among those with marrow infarcts (p less than 0.0001). High levels of HbF, or the presence of alpha- thalassemia, did not protect against marrow infarction. Pulmonary fat embolism was not observed. 99mTc-sulfur colloid marrow imaging was considered to provide more useful information in the initial management of bone pain and swelling in sickle cell crisis than either roentgenographs or conventional 99mTc-methyldiphosphate bone images.


2010 ◽  
Vol 86 (3) ◽  
pp. 309-310 ◽  
Author(s):  
Pascal Rossi ◽  
Marielle Curiel ◽  
Anne Laurence Demoux ◽  
Denis Bagneres ◽  
Régis Costello ◽  
...  

2017 ◽  
Vol 7 (4) ◽  
pp. 42-50 ◽  
Author(s):  
Eduardo Pelegrineti Targueta ◽  
André Carramenha de Góes Hirano ◽  
Fernando Peixoto Ferraz de Campos ◽  
João Augusto dos Santos Martines ◽  
Silvana Maria Lovisolo ◽  
...  

Transfusion ◽  
2021 ◽  
Author(s):  
Mohammad Barouqa ◽  
James Szymanski ◽  
Randin Nelson ◽  
Sebastian Jofre ◽  
Monika Paroder

Blood ◽  
1982 ◽  
Vol 60 (6) ◽  
pp. 1411-1419
Author(s):  
PF Milner ◽  
M Brown

Bone marrow infarction was investigated by 99mTc-sulfur colloid imaging in 42 patients with sickle cell anemia (SS) over a period of 2 yr. Marrow defects were demonstrated in 28 patients (66.6%), and in 15 (aged 19--52 yr), they were matched by roentgenographic evidence of medullary bone infarction. Repeated images showed no change in the size or site of these defects. Among 13 patients (aged 6--32 yr), all in crisis when initially examined, marrow defects were not associated with roentgenographic changes, and in many cases, repeated images showed resolution or decrease in size of the defects in 3--6 mo, even if the limb had been swollen and the marrow defect large. Among 14 patients (aged 18--36 yr), all asymptomatic at the time of study, no defects were found. Comparison of hematologic variables revealed a higher mean hemoglobin and hematocrit level among those with marrow infarcts (p less than 0.0001). High levels of HbF, or the presence of alpha- thalassemia, did not protect against marrow infarction. Pulmonary fat embolism was not observed. 99mTc-sulfur colloid marrow imaging was considered to provide more useful information in the initial management of bone pain and swelling in sickle cell crisis than either roentgenographs or conventional 99mTc-methyldiphosphate bone images.


2021 ◽  
Vol 14 (1) ◽  
pp. e238317
Author(s):  
Nibash Budhathoki ◽  
Sunita Timilsina ◽  
Bebu Ram ◽  
Douglas Marks

Prevalence of haemoglobin sickle-β+ thalassaemia (Hb S/β+thal) is variable with geography ranging from 0.2% to 10% among sickle cell patients. Clinical presentation of Hb S/β+thal patients depends on HbA level, with milder disease often going undiagnosed. However, rarely these patients can present with a fulminant vaso-occlusive crisis (VOC). Given VOC can present with non-specific symptoms, the diagnosis and treatment is often delayed. Here, we present a patient who initially developed altered mental status, pancytopenia and multiorgan failure due a critical VOC resulting in bone marrow necrosis and fat embolism. Subsequent workup confirmed that our patient had Sickle-β+ thalassaemia, which had gone undiagnosed, despite subclinical evidence of haemolysis on routine lab work for years. Following diagnosis and initiation of RBC exchange, he improved significantly and was discharged home. High index of suspicion and bone marrow biopsy is vital for early diagnosis and management of this rare condition.


2021 ◽  
Vol 86 ◽  
pp. 102508
Author(s):  
Melissa Azul ◽  
Surbhi Shah ◽  
Sarah Williams ◽  
Gregory M. Vercellotti ◽  
Alexander A. Boucher

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