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R. D.
Hanmante1, K. S. Dhumure2, K. D. Sawaimul3,
S. W. Chopde2, N.R. Kumbhakarna4, R.S.Bindu5
1Assistant
Professor, Dept. of Pathology, Dr Shankarrao Chavan Government Medical
College, Nanded (MS) INDIA.
2Resident,
Dept. of Pathology, Government Medical College, Aurangabad (MS) INDIA.
3Department
of Pathology, Government Medical College, Aurangabad (MS) INDIA.
4Professor,
Dept. of Pathology, Government Medical College, Aurangabad (MS) INDIA.
5Head
& Professor, Dept. of Pathology, Government Medical College, Aurangabad
(MS) INDIA
Academic Editor: Dr.
Pawar D.D.
Vasoocclusive crisis
or sickle cell crisis is a common painful complication of sickle cell
disease in adolescent & adult. Acute episodes of severe pain (crises)
are the primary reason that these patients seek medical care in hospital
emergency department. Delay or ignorance to this condition is fatal.
It is a retrospective
study of 5 cases. These cases were brought dead to casualty at
Government Medical College & Hospital, Aurangabad. Of these 5 cases, 3
had history of chest pain. After post-mortem examination, the specimens
were sent for histopathological examination. The sections of the
specimens were studied.
Histological
examination shows widespread sickling of red blood cells. .?Aggrevating
factors leads to hypoxemia which further leads to sickling of red blood
cells causing the vasoocclusive crisis & ultimately death of the
patient.
Of these 5 cases, 4
were not investigated haematologically & biochemically previously, the
diagnosis of sickle cell disease made after post-mortem histological
examination.
It is concluded that,
Vasoocclusive crises due to sickle cell can lead to sudden death in
previously undiagnosed sickle cell trait / disease patients.
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