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肺毛细血管瘤病

Capillary haemangiomatosis of the lungs.

作者信息

Wagenvoort C A, Beetstra A, Spijker J

出版信息

Histopathology. 1978 Nov;2(6):401-6. doi: 10.1111/j.1365-2559.1978.tb01734.x.

DOI:10.1111/j.1365-2559.1978.tb01734.x
PMID:730121
Abstract

A case of capillary haemangiomatosis affecting both lungs. The angiomatous growth involved particularly the intralobular fibrous septa and appeared locally aggressive as it had destroyed and obstructed the pulmonary veins and venules. Some pulmonary arteries and bronchi were affected to a lesser extent. Pulmonary venous obstruction, sometimes simulating pulmonary veno-occlusive disease, caused severe haemosiderosis and interstitial fibrosis. The clinical features and the lung biopsy erroneously suggested a diagnosis of primary pulmonary haemosiderosis. No comparable case has been found in the literature.

摘要

一例累及双肺的毛细血管瘤病。血管瘤样生长特别累及小叶内纤维间隔,表现出局部侵袭性,因为它破坏并阻塞了肺静脉和小静脉。一些肺动脉和支气管也有较轻程度的受累。肺静脉阻塞有时类似肺静脉闭塞性疾病,导致严重的含铁血黄素沉着症和间质纤维化。临床特征和肺活检错误地提示原发性肺含铁血黄素沉着症的诊断。文献中未发现类似病例。

相似文献

1
Capillary haemangiomatosis of the lungs.肺毛细血管瘤病
Histopathology. 1978 Nov;2(6):401-6. doi: 10.1111/j.1365-2559.1978.tb01734.x.
2
Pulmonary capillary haemangiomatosis.肺毛细血管瘤病
Diagn Histopathol. 1983 Apr-Jun;6(2):77-84.
3
Invasive pulmonary haemangiomatosis.侵袭性肺血管瘤病
Br J Dis Chest. 1985 Jul;79(3):284-94.
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Multifocal distribution of pulmonary capillary haemangiomatosis.肺毛细血管瘤病的多灶性分布
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Pulmonary veno-occlusive disease and pulmonary capillary hemangiomatosis: a clinicopathologic study of 35 cases.肺静脉闭塞病和肺毛细血管瘤病:35例临床病理研究
Am J Surg Pathol. 2006 Jul;30(7):850-7. doi: 10.1097/01.pas.0000209834.69972.e5.
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Familial pulmonary capillary hemangiomatosis resulting in primary pulmonary hypertension.导致原发性肺动脉高压的家族性肺毛细血管血管瘤病。
Ann Intern Med. 1988 Jul 15;109(2):106-9. doi: 10.7326/0003-4819-109-2-106.
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Pulmonary capillary haemangiomatosis diagnosed during life.生前诊断的肺毛细血管瘤病
Histopathology. 1989 Feb;14(2):212-4. doi: 10.1111/j.1365-2559.1989.tb02131.x.
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Pulmonary capillary hemangiomatosis.肺毛细血管瘤病
Hum Pathol. 1986 Nov;17(11):1144-50. doi: 10.1016/s0046-8177(86)80420-8.
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Pulmonary capillary hemangiomatosis. A report of three cases and a review of the literature.肺毛细血管血管瘤病。三例报告并文献复习。
Am Rev Respir Dis. 1989 Sep;140(3):808-13. doi: 10.1164/ajrccm/140.3.808.

引用本文的文献

1
Pulmonary Capillary Hemangiomatosis as a Rare Underlying Cause of Primary Pulmonary Hypertension: A Case Report in an Adolescent.肺毛细血管血管瘤病作为特发性肺动脉高压的罕见潜在病因:一例青少年病例报告。
Iran J Med Sci. 2024 Jun 1;49(6):394-398. doi: 10.30476/ijms.2024.101215.3385. eCollection 2024 Jun.
2
Solitary pulmonary capillary hemangioma mimicking a preinvasive malignant lesion in an asymptomatic middle-aged female patient.一名无症状中年女性患者的孤立性肺毛细血管血管瘤,酷似浸润前恶性病变。
Int Cancer Conf J. 2022 Aug 3;12(1):14-18. doi: 10.1007/s13691-022-00570-x. eCollection 2023 Jan.
3
Case report: Rescue treatment with add-on selexipag in a preterm infant with suprasystemic pulmonary hypertension, pulmonary capillary hemangiomatosis, and isolated pulmonary vein stenosis.
病例报告:在一名患有系统性高血压、肺毛细血管瘤病和孤立性肺静脉狭窄的早产儿中加用司来帕格进行抢救治疗。
Front Cardiovasc Med. 2022 Dec 9;9:984698. doi: 10.3389/fcvm.2022.984698. eCollection 2022.
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Pulmonary capillary hemangiomatosis: a case series and review of literature.肺毛细血管血管瘤病:病例系列及文献综述
Am J Cardiovasc Dis. 2021 Apr 15;11(2):239-245. eCollection 2021.
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Autopsy study of pulmonary capillary hemangiomatosis with inflammatory cell infiltration into the myocardium.伴有炎性细胞浸润心肌的肺毛细血管瘤病尸检研究
Pulm Circ. 2020 Nov 23;10(4):2045894020960600. doi: 10.1177/2045894020960600. eCollection 2020 Oct-Dec.
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Pulmonary capillary hemangiomatosis-predominant vasculopathy in a patient with rheumatoid arthritis-associated interstitial lung disease: An autopsy report.类风湿关节炎相关间质性肺疾病患者以肺毛细血管血管瘤病为主的血管病变:一份尸检报告
Respir Med Case Rep. 2020 Sep 8;31:101215. doi: 10.1016/j.rmcr.2020.101215. eCollection 2020.
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Pulmonary capillary haemangiomatosis: a distinct entity?肺毛细血管血管瘤病:一种独特的实体?
Eur Respir Rev. 2020 May 27;29(156). doi: 10.1183/16000617.0168-2019. Print 2020 Jun 30.
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Pulmonary vasodilators can lead to various complications in pulmonary "arterial" hypertension associated with congenital heart disease.肺血管扩张剂可导致先天性心脏病相关的肺动脉高压出现各种并发症。
Heart Vessels. 2020 Sep;35(9):1307-1315. doi: 10.1007/s00380-020-01604-1. Epub 2020 Apr 13.
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Capillary Proliferation in Systemic-Sclerosis-Related Pulmonary Fibrosis: Association with Pulmonary Hypertension.系统性硬化症相关肺纤维化中的毛细血管增生:与肺动脉高压的关联
ACR Open Rheumatol. 2019 Mar 15;1(1):26-36. doi: 10.1002/acr2.1003. eCollection 2019 Mar.
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Novel EIF2AK4 mutations in histologically proven pulmonary capillary hemangiomatosis and hereditary pulmonary arterial hypertension.组织学证实的肺毛细血管血管瘤病和遗传性肺动脉高压中的新型 EIF2AK4 突变。
BMC Med Genet. 2019 Nov 11;20(1):176. doi: 10.1186/s12881-019-0915-7.