Telomere biology disorder presented with de novo pneumocystis jirovecii pneumonia: A case report [0.03%]
端粒生物学障碍所致新生肺炎双球菌性肺炎1例报告
Alaa K Hamad,Nagham Joudeh,Ashraf M Saeed et al.
Alaa K Hamad et al.
Introduction: and Importance: Telomere biology disorder (TBD), which is a genetic disorder marked by mutations in telomere-maintenance genes, leading to shortened telomere, accelerated aging, and multi-systems effects inc...
Characterization of alpha-1 antitrypsin in a Pi∗ZZ patient with emphysema: a case report [0.03%]
Pi∗ZZ抗胰蛋白酶异常的肺气肿患者特征分析：个案报告
Arturo Olivares Rivera,Julia Held,Julia Beimdiek et al.
Arturo Olivares Rivera et al.
Background: Lung disease severity and progression vary widely among individuals with severe alpha-1 antitrypsin deficiency (AATD; Pi∗ZZ, Glu342Lys). In addition to low levels of polymerized Z mutant AAT (Z-AAT), this var...
Regorafenib pulmonary toxicity: A case of cavitary lung disease and ARDS treated with infliximab [0.03%]
瑞戈非尼所致肺毒性：一例空洞型肺疾病和急性呼吸窘迫综合征应用英夫利昔单抗治疗的病例报告
Michael Dong,Mackenzie Kramer,Tanmay Gandhi et al.
Michael Dong et al.
Regorafenib-induced pneumonitis and acute respiratory distress syndrome (ARDS) are rare and poorly characterized toxicities. We describe a 43-year-old male with metastatic colorectal cancer who developed hypoxic respiratory failure after tw...
Osimertinib-induced aplastic anemia after curative surgery for EGFR-mutant lung adenocarcinoma [0.03%]
表皮生长因子受体突变型肺腺癌根治术后出现的奥希替尼致重型再生障碍性贫血
Tomoyuki Kawamura,Kenji Minagi,Syuntaro Kawabata et al.
Tomoyuki Kawamura et al.
Osimertinib, a third-generation epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI), is widely used to treat EGFR-mutated non-small cell lung cancer (NSCLC) because of its high efficacy and favourable safety profile. Howev...
Sleep-disordered breathing in Prader-Willi syndrome: Two illustrative examples [0.03%]
普拉德-威利综合征睡眠呼吸障碍的两例分析
Abir Bouhamdi,David Gozal,Yassin Chefchaou et al.
Abir Bouhamdi et al.
Introduction: Prader-Willi syndrome (PWS) is a genetic disorder characterized by hypothalamic dysfunction, resulting in a combination of neurodevelopmental, metabolic, and behavioral abnormalities. Sleep disorders are fre...
When extubation turns fatal: Delayed hemoptysis from negative pressure pulmonary hemorrhage [0.03%]
当拔管致死时：负压肺出血导致的延迟性咯血
Mohammed AbuBaha,Hossam Salameh,Wael Hashem et al.
Mohammed AbuBaha et al.
Negative pressure pulmonary hemorrhage (NPPH) is a rare but serious complication following upper airway obstruction, often due to forceful inspiratory efforts. We report a case of a 25-year-old diabetic male who developed sudden hemoptysis ...
Life-threatening airway stenosis due to Scedosporium infection during nontuberculous mycobacteria treatment: A case report [0.03%]
由链格孢菌感染导致的非结核分枝杆菌治疗期间威胁生命的气道狭窄一例报告
Ayako Kurosaki,Naoko Mato,Akinaga Iijima et al.
Ayako Kurosaki et al.
Fungal pathogens generally grow in the pulmonary parenchyma, but occasionally involve the bronchial wall. A 73-year-old female was admitted to our hospital with dyspnea and a critical endobronchial fungal infection. Because the central airw...
A rare case of upper airway obstruction due to laryngeal leech infestation in a 1-year-old child [0.03%]
一例1岁幼儿喉部感染水蛭导致上呼吸道阻塞的罕见病例报告
Tsion Haile Woldemariam,Fitsum Alemayehu Siyum,Robel Tibebu Kasaye et al.
Tsion Haile Woldemariam et al.
Leech infestation of the upper airway is a rare but potentially life-threatening event, particularly in young children from rural areas exposed to untreated water sources. We report a case of a 1-year-old boy presenting with acute upper air...
Multidetector computed tomography angiography predicts the need for bronchial artery embolization in hemoptysis: A retrospective cohort study of 32 patients [0.03%]
多检测器CT血管造影可预测大咯血支气管动脉栓塞的指征：32例患者的回顾性队列研究
Haruyasu Sakuranaka,Yosuke Nemoto,Ryota Nakayama et al.
Haruyasu Sakuranaka et al.
Background: Bronchial artery embolization (BAE) is the standard intervention for severe hemoptysis, yet predicting which patients will require BAE remains challenging. We evaluated whether multidetector computed tomograph...
Congenital tracheobronchomegaly (Mounier-Kuhn syndrome) in a 70-year-old nonsmoking male: A rare presentation in a low-resource setting [0.03%]
70岁不吸烟男性特发性主支气管过长症一例报告
Yousif Aboaziza,Eiman Aboaziza,Rabha E Almahdi et al.
Yousif Aboaziza et al.
Background: Mounier-Kuhn Syndrome (MKS), or congenital tracheobronchomegaly, is a rare disorder characterized by dilation of the trachea and main bronchi due to the atrophy of elastic and smooth muscle fibers. Though ofte...