Chronic Splenomegaly

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Chronic myeloid leukemia with marked splenomegaly and pseudo-Gaucher cells

which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. A 17-year-old boy with no specific medical history presented with abdominal distension. A complete blood analysis revealed a leukocyte count of 151.6×10 9 /L. A contrast-enhanced abdominal computed tomography image showed marked splenomegaly (A) and mildly e...

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Splenomegaly, hypersplenism, and hereditary disorders with splenomegaly

Splenomegaly, sometimes of massive extent, occurs in a large number of hereditary diseases, some relatively prevalent and others, rare to ultra-rare. Because physicians are often unfamiliar with the less common disorders, patients may suffer because of diagnostic delay or diagnostic error and may undergo invasive, non-innocuous procedures such as splenectomy that are potentially avoidable were ...

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A Case Report of Splenomegaly Due to Chronic Salmonellosis in a Three Months Old Holstein Calf

Objective: Salmonellosis is a bacterial disease with a rising prevalence in the cattle industry. It is most common in dairy calves one to ten weeks of age. Salmonellosis has a serious economic impact on the cattle industry worldwide. Methods: In May 2013, a three months old male Holstein calf with the history of lateral recumbency was referred to veterinary hospital with severe depression, cach...

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A Case Report of Splenomegaly Due to Chronic Salmonellosis in a Three Months Old Holstein Calf

Objective: Salmonellosis is a bacterial disease with a rising prevalence in the cattle industry. It is most common in dairy calves one to ten weeks of age. Salmonellosis has a serious economic impact on the cattle industry worldwide. Methods: In May 2013, a three months old male Holstein calf with the history of lateral recumbency was referred to veterinary hospital with severe depression, cach...

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ژورنال

عنوان ژورنال: Proceedings of the Royal Society of Medicine

سال: 1937

ISSN: 0035-9157

DOI: 10.1177/003591573703100110