Is it a sea-blue histiocyte?
نویسنده
چکیده
In the “Images in Hematology’’ section of the Journal, And›ç et al. [1] briefly presented sea-blue histiocytes in a 45-year-old woman with type B Niemann-Pick disease [2,3]. I believe the cell photographed by the authors is fairly typical for Niemann-Pick disease with few nuclear remnants and superimposed lymphocytes. In my opinion, it is not typical for sea-blue histiocytes. We have seen sea-blue histiocyte cells, congenital and acquired, on several occasions [4] in bone marrow and the spleen, as well as in liver aspiration biopsies. Although a few granules may be seen rarely in a few sea-blue histiocytes, they are typically blue cells. Ceroid content determination would be helpful in questionable cells.
منابع مشابه
Ceroid histiocytosis of the spleen in hyperlipemia: relationship to the syndrome of the sea-blue histiocyte.
Rywlin, Arkadi M., Lopez-Gomez, Alfredo, Tachmes, Pablo, and Pardo, Victoriano: Ceroid histiocytosis of the spleen in hyperlipemia: Relationship to the syndrome of the sea-blue histiocyte. Amer. J. Clin. Path. 56: 572-579, 1971. Morphologic findings in a patient with primary, type 5 hyperlipoproteinemia of Fredrickson and Lees, reported for the first time, include marked splenomegaly with exten...
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The syndrome of sea-blue histiocyte, hepatic porphyria, and infectious mononucleosis occurring simultaneously in a young girl is described. The cytochemical staining character of the bone marrow histiocytes strongly suggested that the storage material was glycolipid. The possible relationship between the multiple disorders in the same patient is discussed.
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A patient with sea-blue histiocytosis in spleen and bone marrow with an accompanying hyperlipidaemia is described. The hyperlipidaemia was due to an increase in "free" cholesterol, lecithin, and triglycerides. Despite these findings lecithin-cholesterol acyl transferase activity was normal. Although the precise biochemical defect was not identified, there was a failure of transport of cholester...
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A 27-year-old Indian woman at 23 weeks' gestation presented with decompensated liver cirrhosis, coagulopathy, restrictive lung disease with cor pulmonale and preeclampsia. She was diagnosed to have sea-blue histiocyte syndrome (SBHS) at the age of 13 years and was treated conservatively. There was worsening liver, respiratory and bone marrow function as the pregnancy progressed. She underwent a...
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The authors present the case of a 73 year old man with primary myelofibrosis, pulmonary fibrosis, and acquired sea-blue histiocytosis, who died of respiratory failure. Pathology of the lungs revealed infiltration by sea-blue histiocytes, and fibrosis in the alveolar septa, and clumps of these cells filling the alveolar spaces. Megakaryocytes were also occasionally observed in the alveolar capil...
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ورودعنوان ژورنال:
- Turkish journal of haematology : official journal of Turkish Society of Haematology
دوره 25 1 شماره
صفحات -
تاریخ انتشار 2008