Zobrazeno 1 - 10
of 354
pro vyhledávání: '"Pulmonary capillary hemangiomatosis"'
Autor:
E. A. Rezukhina, E. A. Devetyarova, A. I. Trapeznikova, E. V. Paschenko, T. V. Martynyuk, A. A. Dyuzhikov
Publikováno v:
Евразийский Кардиологический Журнал, Vol 0, Iss 3, Pp 82-86 (2024)
Our observation demonstrates a case of a 40-year-old female with pulmonary arterial hypertension World Health Organization functional class III, who was admitted to NMRC of Cardiology repeatedly due to disease progression including dyspnea worsening,
Externí odkaz:
https://doaj.org/article/9b46d4661f00406a870639ddf84a836e
Publikováno v:
Open Veterinary Journal, Vol 14, Iss 5, Pp 1216-1223 (2024)
Background: Pulmonary capillary hemangiomatosis (PCH) is an idiopathic disease with the anomalous proliferation of a small capillary-like vessel in the pulmonary tissue, which can lead to a severe form of PH. There are only several cases of PCH descr
Externí odkaz:
https://doaj.org/article/dacfa4cd0fbf492f8f8793013db98f51
Clinical case of a patient with pulmonary capillary hemangiomatosis: rapid progression or lost time?
Publikováno v:
Евразийский Кардиологический Журнал, Vol 0, Iss 4, Pp 74-78 (2021)
The article describes a clinical case of a 37-year-old patient with pulmonary capillary hemangiomatosis of functional class IV according to the WHO classification with difficulties of diagnostic search and features of PAH-specific therapy.Pulmonary a
Externí odkaz:
https://doaj.org/article/a351369002a048cc9b6da6b0748e36ca
A case of early diagnosis of pulmonary capillary hemangiomatosis in a worker with exposure to silica
Autor:
Chang Dong Yeo, Deokjae Han, Jongmin Lee, Woo-Baek Chung, Jung Im Jung, Kyo-Young Lee, Tae-Jung Kim, Woori Jang, Myungshin Kim, Ji Young Kang
Publikováno v:
BMC Pulmonary Medicine, Vol 19, Iss 1, Pp 1-7 (2019)
Abstract Background Pulmonary capillary hemangiomatosis (PCH) is a progressive and refractory vascular disease in the lung. Pulmonary hypertension is frequently combined with PCH when capillary proliferation invades to nearby pulmonary vascular syste
Externí odkaz:
https://doaj.org/article/9d6cf145248b455c943a77da268d5bae
Autor:
Lavinia Neubert, Paul Borchert, Hoen‐Oh Shin, Friedemann Linz, Willi L Wagner, Gregor Warnecke, Florian Laenger, Axel Haverich, Helge Stark, Marius M Hoeper, Mark Kuehnel, Maximilian Ackermann, Danny Jonigk
Publikováno v:
The Journal of Pathology: Clinical Research, Vol 5, Iss 2, Pp 108-114 (2019)
Abstract Pulmonary veno‐occlusive disease (PVOD) is a rare lung disease characterized by fibrotic narrowing of pulmonary veins leading to pulmonary hypertension (PH) and finally to death by right heart failure. PVOD is often accompanied by pulmonar
Externí odkaz:
https://doaj.org/article/f23f93df2500491d8562778f59ad5968
Akademický článek
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Autor:
Junichi Nakamura, Ichizo Tsujino, Gaku Yamamoto, Toshitaka Nakaya, Kei Takahashi, Hirokazu Kimura, Takahiro Sato, Taku Watanabe, Shimpei Nakagawa, Noriyuki Otsuka, Hiroshi Ohira, Satoshi Konno
Publikováno v:
Respiratory Medicine Case Reports, Vol 31, Iss , Pp 101215- (2020)
Pulmonary capillary hemangiomatosis (PCH) is a rare cause of pulmonary hypertension (PH) associated with poor prognosis. Clinically, it is characterized by severe hypoxemia, centrilobular ground-glass opacities on computed tomography, and pulmonary c
Externí odkaz:
https://doaj.org/article/c6fb3d4ec1fa422db3680deac80ab399
Autor:
Marjolein Lisette den Toom, Guy Grinwis, Robert-Jan van Suylen, Susanne Adetokunbo Boroffka, Pim de Jong, Frank Geurt van Steenbeek, Viktor Szatmári
Publikováno v:
Acta Veterinaria Scandinavica, Vol 60, Iss 1, Pp 1-8 (2018)
Abstract Background Pulmonary veno-occlusive disease (PVOD) is a rare cause of pulmonary arterial hypertension (PAH) in humans and can be classified in idiopathic, heritable, drug and radiation-induced, and associated with connective tissue disease o
Externí odkaz:
https://doaj.org/article/21c45ae913324de29185b2293ea9c5da
Publikováno v:
Lung India, Vol 35, Iss 3, Pp 231-236 (2018)
Diffuse parenchymal lung diseases (DPLDs) encompass a variety of restrictive and obstructive lung pathologies. In this article, the authors discuss a series of rare pulmonary entities and their high-resolution computed tomography imaging appearances,
Externí odkaz:
https://doaj.org/article/400c9880ac1c4651bbb2668f73f8cff9
Publikováno v:
Lung India, Vol 36, Iss 2, Pp 157-159 (2019)
Pulmonary capillary hemangiomatosis (PCH) is a rare cause of primary pulmonary hypertension (PPH) diagnosed in children and young adults with a nonspecific clinical presentation of dyspnea, cough, chest pain, and fatigue. It is characterized by exten
Externí odkaz:
https://doaj.org/article/3ce9b0b1a44c470fb666b6b7474e7678