Results 51 to 60 of about 9,034 (208)

Pulmonary Alveolar Microlithiasis, a Rare Cause of Progressive Restrictive Lung Disease

Respirology Case Reports, Volume 14, Issue 2, February 2026.
We present a case of a young patient with pulmonary alveolar microlithiasis, initially misdiagnosed and treated for tuberculosis. Transbronchial lung biopsy revealed intralveolar calcifications confirming the diagnosis. The patient was treated symptomatically and advised long‐term oxygen therapy during episodes of breathlessness.
Shahzeen Irshad, Kinza Asghar, Shehran Majid, Muhammad Umer Ishaq, Maryam Asghar, Syed Muneeb Ahmad, Pooja Shah   +6 more
wiley   +1 more source

Lipoid proteinosis [PDF]

, 2008
OBJETIVO: Apresentar as características clínicas, tratamento cirúrgico e achado histológico de um caso de lipoidoproteinose. DESCRIÇÃO DO CASO: Criança do sexo masculino, cinco anos de idade, branco, que procurou atendimento odontológico na Universidade.
BRESAOLA, Marco Dapieve, CASTILHO, Aline Rogéria F., FRANCISCHONE, Leda Aparecida, KAWAKAMI, Roberto Yoshio, MARTA, Gustavo Nader, MARTA, Sara Nader, MATSUMOTO, Mariza Akemi   +6 more
core   +2 more sources

Fast-Track Extubation in a Patient Undergoing Whole Lung Lavage: A Case Report

Annals of Cardiac Anaesthesia
Pulmonary alveolar proteinosis (PAP) is a rare pulmonary pathology characterized by the accumulation of surfactant within type II alveolar epithelial cells.
Gade Sandeep, Subrata K. Singha, Anil Gupta, Keerthi Chinnadurai, Harishchandra Gupta   +4 more
doaj   +1 more source

Alveolar proteinosis of genetic origins

European Respiratory Review, 2020
Pulmonary alveolar proteinosis (PAP) is a rare form of chronic interstitial lung disease, characterised by the intra-alveolar accumulation of lipoproteinaceous material. Numerous conditions can lead to its development.
Alice Hadchouel, David Drummond, Rola Abou Taam, Muriel Lebourgeois, Christophe Delacourt, Jacques de Blic   +5 more
doaj   +1 more source

Pulmonary alveolar proteinosis - a case report [PDF]

, 2014
Efst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á hlekkinnPróteinútfellingar í lungnablöðrum (pulmonary alveolar proteinosis, PAP) eru oftast af óþekktum orsökum en meingerð sjúkdómsins er rakin til skertrar átfrumuvirkni í ...
Eyþór Björnsson, Felix Valsson, Hrönn Harðardóttir, Ragnheiður M. Jóhannesdóttir, Sigfús Nikulásson, Steinn Jónsson, Tómas Guðbjartsson, Ólöf R. Ámundadóttir   +7 more
core  

Von Hippel-Lindau protein is required for optimal alveolar macrophage terminal differentiation, self-renewal, and function [PDF]

, 2018
The rapid transit from hypoxia to normoxia in the lung that follows the first breath in newborn mice coincides with alveolar macrophage (AM) differentiation.
Brandi, Paola, Conde-Garrosa, Ruth, Conejero, Laura, Enamorado, Michel, Gomez, Manuel-Jose, Guilliams, Martin, Izquierdo, Helena M, Jimenez-Carretero, Daniel, Martin-Puig, Silvia, Martinez-Cano, Sarai, Priego, Elena, Sanchez, Iris, Sancho, David   +12 more
core   +4 more sources

Autoimmune pulmonary alveolar proteinosis prior to myelodysplastic syndrome

Respirology Case Reports, 2020
We report the first case of autoimmune pulmonary alveolar proteinosis (PAP) associated with and preceding myelodysplastic syndrome. A 74‐year‐old female with a history of polymyalgia rheumatica presented with six months history of progressive exertional ...
Chuan Tai Foo, Louis Chhor, Francis Thien   +2 more
doaj   +1 more source

Intestinal Behçet’s disease complicated by myelodysplastic syndrome and secondary pulmonary alveolar proteinosis: a case report

BMC Gastroenterology, 2021
Background Gastrointestinal lesions, which sometimes develop in Behçet’s disease (BD), are referred to as intestinal BD. Although rare, intestinal BD can be accompanied by myelodysplastic syndrome (MDS) with abnormal karyotype trisomy 8, which is ...
Hiroshi Shimizu, Shuzo Sato, Tomohiro Suzuki, Tomomi Sasajima, Yosuke Takahata, Nobuhiko Shinohara, Kosuke Hideshima, Yuko Yokokawa, Nobuo Matsuhashi, Osamu Ichii, Mayumi Tai, Yutaka Ejiri, Kiori Yano, Takayuki Ikezoe, Hiromasa Ohira, Kiyoshi Migita   +15 more
doaj   +1 more source

Idiopathic desquamative interstitial pneumonia in a child: a case report. [PDF]

, 2014
Desquamative interstitial pneumonia is a rare form of interstitial lung disease in children. Respiratory symptoms appear progressively, are often subtle, and diagnosis is often delayed by a mean of 6 months after onset.
Aubert, J.D., Bressieux-Degueldre, S., Hafen, G., Rochat, I., Rotman, S.   +4 more
core   +1 more source

Responsive liquid metal materials towards unstructured environment

Responsive Materials, Volume 4, Issue 1, February 2026.
Room‐temperature liquid metals integrate conductivity, deformability, and interfacial dynamics, enabling robust performance in unstructured environments. This review highlights key properties, requirements, and applications across in vivo, underwater, natural, space, and radiation settings, with advances in sensing, actuation, thermal regulation, and ...
Bo Yuan, Huaitong Song, Kaiyuan Xiang, Shili Tang, Cailin Liu, Hongzhang Wang   +5 more
wiley   +1 more source