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[Persistent hemoptysis secondary to extensive epithelioid angiosarcoma].

Pulmonary angiosarcoma is an unusual cause of diffuse pulmonary hemorrhage. Angiosarcomas are rare malignant vascular tumors accounting for 1% to 2% of all sarcomas. Angiosarcomas have been detected in nearly all organs, but lung involvement is unusual, accounting for less than 7%. The literature describes approximately 10 isolated cases of primary pulmonary angiosarcoma as opposed to the more common metastatic type. Given that primary and metastatic types are clinicopathologically similar, the presence of a distant primary sarcoma must be ruled out before a diagnosis of primary pulmonary angiosarcoma can be made. A pathological diagnosis requires a finding of polygonal or oval cells with atypical irregular nuclei and vascular spaces lined with such cells surrounded by hemorrhagic phenomena. Immunohistochemical analysis is positive for specific endothelial cell markers such as CD31 and factor VIII, and coexpression of keratin is a frequent finding.

Aged↗

[Dyspnea and hemoptysis in a young woman with unclear renal alterations].

We describe the clinical course and treatment of a young woman diagnosed with tuberous sclerosis. Classical as well as atypical clinical findings are discussed with regards to the differential diagnosis. The most important components of the pathogenesis and the criteria necessary for diagnosis are highlighted. In addition the similarities and differences to lymphangioleiomyomatosis are discussed.

Adult↗

[Hemoptysis].

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Arteriovenous Fistula↗

[Treatment of hemoptysis by embolization of the thoracic arteries with Ethibloc].

Between November 1983 and July 1988 28 patients with haemoptysis were treated by transcatheter embolisation. Clinical follow-up of 22 patients revealed that 5 patients rebled within 21 days after embolization. Haemoptysis ceased completely in the remaining 17 patients. However, 2 patients rebled after 4 and 12 months, respectively. We observed two transient spinal cord injuries, most likely related to spinal cord ischaemia. In the first patient an intercostal artery was embolised with Ethibloc, in the second patient with Gelfoam. In summary, we can say that due to the inherent risk of spinal cord injury, embolisation should be restricted to patients in whom other forms of treatment failed or proved impossible. Ethibloc may be alternatively used for embolisation.

Adult↗

[Severe hemoptysis in pulmonary vasculitis].

A 27-year-old man, in good health but a moderate smoker, suddenly had two episodes of haemoptysis. Routine clinical examination was unremarkable. Erythrocyte sedimentation rate was increased to 34 mm/h. The chest radiography showed ill-defined, contrast-poor infiltrations bilaterally, as well as left hilar enlargement. Lung scintigraphy and pulmonary arteriogram suggested pulmonary embolism, possible from a "pelvic vein spur", i.e. an intimal proliferation due to crossing of the common iliac artery over the pelvic vein. He was placed on oral anticoagulants. Three months later he had another severe haemoptysis, providing the indication for an exploratory thoracotomy. This revealed the left pulmonary artery wall to have inflammatory changes with aneurysmal dilatation. The aneurysm was plicated. Histological examination demonstrated chronic vasculitis as seen in Behçet's syndrome, a diagnosis confirmed by the findings of ulcers of the oral mucosa and the presence of HLA B5 allo-antigens. Immunosuppressive treatment was given with prednisone (1 mg/kg), azathioprine (2.5 mg/kg) and ciclosporin (5 mg/kg). Over the next 12 months there has been only one further haemoptysis.

Adult↗