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首页> 外文期刊>Archives of Pathology & Laboratory Medicine >Alveolar Airspace and Pulmonary Artery Involvement by Extramedullary Hematopoiesis: A Unique Manifestation of Myelofibrosis
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Alveolar Airspace and Pulmonary Artery Involvement by Extramedullary Hematopoiesis: A Unique Manifestation of Myelofibrosis

机译:髓外造血引起的肺泡空域和肺动脉受累:骨髓纤维化的独特表现

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Pulmonary extramedullary hematopoiesis is a rare manifestation of myelofibrosis. We encountered a unique case of pulmonary extramedullary hematopoiesis occurring in a 59-year-old white man, where in addition to the typical foci of interstitial hematopoietic cells, a surgical lung biopsy showed airspace and arterial wall involvement. Airspace foci were associated with acute and organizing alveolar hemorrhage, while within arteries the hematopoietic elements had a striking predilection for the vascular intima. The hematopoietic foci included erythroid precursors, myeloid precursors, and megakaryocytes, which were immunoreactive with hemoglobin, myeloperoxidase, and CD61, respectively. Whether extramedullary hematopoiesis represents in situ embryonic stem cell differentiation or a compensatory seeding of hematopoietic cells from the bone marrow remains to be elucidated. However, familiarity with these findings in the lung could be helpful in uncovering occult hematological disorders accompanied by extramedullary hematopoiesis. Extramedullary hematopoiesis should also be considered as a cause of pulmonary hemorrhage, especially in the setting of myelofibrosis.
机译:肺髓外造血是一种罕见的骨髓纤维化表现。我们遇到了一位59岁的白人发生的肺部髓外造血的独特病例,该病除了典型的间质造血细胞灶外,还进行了外科肺活检,显示有空域和动脉壁受累。空域病灶与急性和有组织的肺泡出血有关,而在动脉内,造血成分对血管内膜的影响尤为明显。造血灶包括红血球前体,骨髓前体和巨核细胞,它们分别与血红蛋白,髓过氧化物酶和CD61发生免疫反应。髓外造血是代表原位胚胎干细胞分化还是来自骨髓的造血细胞代偿性播种仍有待阐明。但是,熟悉肺部这些发现可能有助于发现隐匿性血液系统疾病并伴有髓外造血。髓外造血也应被认为是引起肺出血的原因,尤其是在骨髓纤维化的情况下。

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    《Archives of Pathology & Laboratory Medicine》 |2008年第1期|p.99-103|共5页
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    Irem H. Ozbudak, MD, Konstantin Shilo, MD, Sabine Hale, MD, Nadine S. Aguilera, MD, Jeffrey R. Galvin, MD, Teri J. Franks, MDAccepted for publication July 27, 2007From the Department of Pathology, University of Akdeniz School of Medicine, Antalya, Turkey (Dr Ozbudak), the Departments of Pulmonary and Mediastinal Pathology (Drs Shilo and Franks), Hematopathology (Dr Aguilera), and Radiologic Pathology (Dr Galvin), Armed Forces Institute of Pathology, Washington, DC, the Department of Pathology, St Michaels Hospital, Stevens Point, Wis (Dr Hale), and the Department of Diagnostic Radiology and Pulmonary/Critical Care Medicine, University of Maryland School of Medicine, Baltimore (Dr Galvin).The authors have no relevant financial interest in the products or companies described in this article.Reprints: Konstantin Shilo, MD, Department of Pulmonary and Mediastinal Pathology, Armed Forces Institute of Pathology, 6825 NW 16 St, Washington, DC (e-mail: shilok@afip.osd.mil).,;

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