Respirology Case Reports最新文献

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A Case of Nontuberculous Mycobacterial Pulmonary Disease Complicating Massive Pulmonary Embolism. 非结核性分枝杆菌肺病合并大体积肺栓塞1例。
IF 0.8
Respirology Case Reports Pub Date : 2025-07-24 eCollection Date: 2025-07-01 DOI: 10.1002/rcr2.70292
Yasuyuki Hayashi, Akihiko Sokai, Toshiyuki Iwata, Yuki Sakai, Naoaki Yasuda, Takashi Nishimura
{"title":"A Case of Nontuberculous Mycobacterial Pulmonary Disease Complicating Massive Pulmonary Embolism.","authors":"Yasuyuki Hayashi, Akihiko Sokai, Toshiyuki Iwata, Yuki Sakai, Naoaki Yasuda, Takashi Nishimura","doi":"10.1002/rcr2.70292","DOIUrl":"10.1002/rcr2.70292","url":null,"abstract":"<p><p>A 39-year-old man presented with fever and dyspnoea for 1 week. Imaging suggested bacterial pneumonia with infiltrates in the right lung. However, the symptoms persisted despite antibiotics. Bronchoscopy revealed coagulation necrosis, and enhanced computed tomography identified a large thrombus in the right pulmonary artery, leading to a diagnosis of pulmonary infarction. The patient was treated with direct oral anticoagulants. Two years later, new nodular lesions with cavities were observed in the upper lobe of the right lung. Bronchoscopy revealed a <i>Mycobacterium avium</i> infection. We hypothesise that nontuberculous mycobacterial (NTM) pulmonary disease may complicate chronic pulmonary embolism.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"13 7","pages":"e70292"},"PeriodicalIF":0.8,"publicationDate":"2025-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12289390/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144733830","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case of Haemophilus influenzae Colonisation in Bronchiectasis Following COVID-19: Post-COVID-19 Bronchiectasis as a Structural Hotbed for Chronic Airway Infections. COVID-19后支气管扩张中流感嗜血杆菌定植的一例:COVID-19后支气管扩张是慢性气道感染的结构性温床
IF 0.8
Respirology Case Reports Pub Date : 2025-07-23 eCollection Date: 2025-07-01 DOI: 10.1002/rcr2.70287
Issei Oi, Yuta Okada, Naoki Fujimoto, Saiki Yoshimura, Shogo Toyama, Takanori Ito, Takuma Imakita, Osamu Kanai, Kohei Fujita, Kiminobu Tanizawa
{"title":"A Case of <i>Haemophilus influenzae</i> Colonisation in Bronchiectasis Following COVID-19: Post-COVID-19 Bronchiectasis as a Structural Hotbed for Chronic Airway Infections.","authors":"Issei Oi, Yuta Okada, Naoki Fujimoto, Saiki Yoshimura, Shogo Toyama, Takanori Ito, Takuma Imakita, Osamu Kanai, Kohei Fujita, Kiminobu Tanizawa","doi":"10.1002/rcr2.70287","DOIUrl":"10.1002/rcr2.70287","url":null,"abstract":"<p><p>Coronavirus Disease 2019 (COVID-19) can lead to respiratory sequelae, including bronchiectasis. While bronchiectasis following tuberculosis is a breeding ground for many bacterial infections/colonisation, there are few reports of bronchiectasis following COVID-19 being a hotbed for bacterial infection/colonisation. We present a case of a 69-year-old female who developed bronchiectasis following COVID-19 pneumonia. The patient had no abnormal findings on chest CT scan for 5 years before COVID-19. She developed persistent cough and sputum after COVID-19 and chest CT just after COVID-19 revealed new bronchiectasis. One year later, she was introduced to our department for repeating exacerbation of chronic respiratory infection, and <i>Haemophilus influenzae</i> was detected in sputum. This case highlights the potential for <i>H. influenzae</i> to infect/colonise in post-COVID-19 bronchiectasis. While there have been few reports of chronic airway infection complicating bronchiectasis after COVID-19 until now, long-term respiratory follow-up and management of bacterial colonisation are crucial in these patients in the future. This case suggests that COVID-19 can predispose individuals to bacterial infection in the setting of bronchiectasis, emphasising the need for vigilance in post-COVID-19 airway management.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"13 7","pages":"e70287"},"PeriodicalIF":0.8,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12286885/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144709378","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Breathing With Half a Pulmonary Circuit: Three Cases of Unilateral Pulmonary Artery Agenesis. 半肺循环呼吸:单侧肺动脉发育不全3例。
IF 0.8
Respirology Case Reports Pub Date : 2025-07-22 eCollection Date: 2025-07-01 DOI: 10.1002/rcr2.70280
Vignesh Kumar Kathiresan, Benjamin Earnest Williams, V S Aswith Chowdary Jonnalagadda
{"title":"Breathing With Half a Pulmonary Circuit: Three Cases of Unilateral Pulmonary Artery Agenesis.","authors":"Vignesh Kumar Kathiresan, Benjamin Earnest Williams, V S Aswith Chowdary Jonnalagadda","doi":"10.1002/rcr2.70280","DOIUrl":"10.1002/rcr2.70280","url":null,"abstract":"<p><p>Unilateral pulmonary artery atresia (UPAA) is a rare congenital anomaly marked by the absence of one of the pulmonary arteries. This article examines three instances of UPAA, predominantly affecting the right side, although one case involved the left side. Common characteristics included hemoptysis, observed in two patients-one with a chronic history necessitating embolization and another with a mild, recent onset. The third case was identified incidentally during a preoperative evaluation. All cases demonstrated varying degrees of ipsilateral lung volume reduction and associated interstitial changes or fibrosis. UPAA can be asymptomatic or present with hemoptysis, recurrent infections, or breathlessness. Diagnosis relies on computed tomography pulmonary angiography (CTPA) or magnetic resonance (MR) angiography. Management ranges from observation to embolization or pneumonectomy in severe cases. Mortality is around 7%, with pulmonary hypertension and haemorrhage being major prognostic factors.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"13 7","pages":"e70280"},"PeriodicalIF":0.8,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12283216/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144700025","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Percutaneous Thrombectomy Using AngioJet in Acute Pulmonary Embolism With Clot in Transit. 血管喷射术在急性肺栓塞中的应用。
IF 0.8
Respirology Case Reports Pub Date : 2025-07-22 eCollection Date: 2025-07-01 DOI: 10.1002/rcr2.70296
Atif Saleem Siddiqui
{"title":"Percutaneous Thrombectomy Using AngioJet in Acute Pulmonary Embolism With Clot in Transit.","authors":"Atif Saleem Siddiqui","doi":"10.1002/rcr2.70296","DOIUrl":"10.1002/rcr2.70296","url":null,"abstract":"<p><p>Percutaneous pulmonary thrombectomy using the AngioJet device is a feasible option for the management of acute pulmonary embolism with a clot in transit in selected high-risk patients. Further large-scale studies are needed to better establish the safety and efficacy of percutaneous thrombectomy for clot in transit in high-risk populations.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"13 7","pages":"e70296"},"PeriodicalIF":0.8,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12284313/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144700027","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case of Stevens-Johnson Syndrome Triggered by Methicillin-Resistant Staphylococcus aureus Infection During Pembrolizumab Treatment for Lung Squamous Cell Carcinoma. 派姆单抗治疗肺鳞状细胞癌期间耐甲氧西林金黄色葡萄球菌感染引发史蒂文斯-约翰逊综合征1例
IF 0.8
Respirology Case Reports Pub Date : 2025-07-22 eCollection Date: 2025-07-01 DOI: 10.1002/rcr2.70290
Yusuke Irie, Kazutoshi Isobe, Ryogo Ohashi, Kensuke Namba, Misa Iwayanagi, Hiromasa Sakurai, Daiki Sakai, Kenta Takashima, Yu Murakami, Kaichi Kaneko, Nobuharu Mitsuyama, Hiroki Wakabayashi, Yasuo Matsuzawa
{"title":"A Case of Stevens-Johnson Syndrome Triggered by Methicillin-Resistant <i>Staphylococcus aureus</i> Infection During Pembrolizumab Treatment for Lung Squamous Cell Carcinoma.","authors":"Yusuke Irie, Kazutoshi Isobe, Ryogo Ohashi, Kensuke Namba, Misa Iwayanagi, Hiromasa Sakurai, Daiki Sakai, Kenta Takashima, Yu Murakami, Kaichi Kaneko, Nobuharu Mitsuyama, Hiroki Wakabayashi, Yasuo Matsuzawa","doi":"10.1002/rcr2.70290","DOIUrl":"10.1002/rcr2.70290","url":null,"abstract":"<p><p>Pembrolizumab can cause extremely serious skin disorders with high mortality rates, such as Stevens-Johnson syndrome (SJS), with most cases occurring early after immune checkpoint inhibitor treatment. This report describes a patient that developed SJS triggered by methicillin-susceptible <i>Staphylococcus aureus</i> (MSSA) infection 8 months into pembrolizumab treatment for lung squamous cell carcinoma. A 74-year-old male developed fever, oral mucosal damage, oedematous erythema with erosions predominantly in the trunk and renal dysfunction 8 months after starting pembrolizumab monotherapy for the postoperative recurrence of lung squamous cell carcinoma. SJS was diagnosed and the patient was hospitalised. Cultures of purulent exudates from the facial skin and sputum revealed MSSA. The skin and mucosa findings did not improve despite steroid pulse therapy, but gradual improvements were seen after treatment with ampicillin-sulbactam, vancomycin and four sessions of plasma exchange therapy.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"13 7","pages":"e70290"},"PeriodicalIF":0.8,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12283215/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144700023","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bilateral Massive Pleural Effusion Caused by Spinal Instability in Diffuse Idiopathic Skeletal Hyperostosis: A Rare but Potentially Serious Complication of Spinal Fracture. 弥漫性特发性骨骼肥厚症中脊柱不稳定引起的双侧大量胸腔积液:一种罕见但潜在严重的脊柱骨折并发症。
IF 0.8
Respirology Case Reports Pub Date : 2025-07-22 eCollection Date: 2025-07-01 DOI: 10.1002/rcr2.70277
Keisuke Nishikawa, Tetsuo Tani, Takeshi Fujii, Kota Ishioka, Hideaki Imabayashi, Saeko Takahashi
{"title":"Bilateral Massive Pleural Effusion Caused by Spinal Instability in Diffuse Idiopathic Skeletal Hyperostosis: A Rare but Potentially Serious Complication of Spinal Fracture.","authors":"Keisuke Nishikawa, Tetsuo Tani, Takeshi Fujii, Kota Ishioka, Hideaki Imabayashi, Saeko Takahashi","doi":"10.1002/rcr2.70277","DOIUrl":"10.1002/rcr2.70277","url":null,"abstract":"<p><p>A 71-year-old man with diffuse idiopathic skeletal hyperostosis (DISH) underwent posterior spinal fixation for a thoracic vertebral fracture at a fused segment, sustained as a result of a fall. One month postoperatively, he was readmitted due to bilateral massive pleural effusions and increased displacement at the fracture site compared to the immediate postoperative state. The effusions were exudative and lymphocyte-predominant. Further evaluation suggested that inflammation and pleural irritation due to spinal instability were the likely causes. Revision fixation led to the resolution of the effusions. Vertebral fractures caused by low-energy trauma, such as a fall, rarely result in spinal instability severe enough to cause pleural effusion, even in cases of nonunion. However, patients with DISH are more prone to highly unstable fractures due to spinal ankylosis and bone fragility. Even after surgical fixation, such fractures may progress to further instability. We report a case in which this instability led to localised inflammation and pleural irritation, ultimately resulting in bilateral pleural effusions. DISH is commonly seen in older adults and has been associated with obesity and diabetes mellitus. Its prevalence is reportedly increasing. Therefore, both internists and orthopaedic surgeons should be aware of the potential for similar cases and consider spinal instability related to DISH in the differential diagnosis and management of unexplained pleural effusions.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"13 7","pages":"e70277"},"PeriodicalIF":0.8,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12284312/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144700024","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Endobronchial Lipoma: A Hidden Obstruction Behind Chronic Cough. 支气管内脂肪瘤:慢性咳嗽背后的隐藏障碍。
IF 0.8
Respirology Case Reports Pub Date : 2025-07-22 eCollection Date: 2025-07-01 DOI: 10.1002/rcr2.70291
Zeinab El Mawla, Bilal Damen
{"title":"Endobronchial Lipoma: A Hidden Obstruction Behind Chronic Cough.","authors":"Zeinab El Mawla, Bilal Damen","doi":"10.1002/rcr2.70291","DOIUrl":"10.1002/rcr2.70291","url":null,"abstract":"<p><p>Endobronchial lipomas are rare, benign tumours that arise from the submucosal fat of the bronchial wall and account for less than 0.5% of all lung tumours. These tumours can present with non-specific respiratory symptoms, often mimicking common pulmonary conditions such as asthma, COPD, or infections, making diagnosis challenging. We present the case of a 54-year-old female smoker who experienced a three-month history of chronic productive cough, dyspnea and recurrent respiratory infections. During this period, she was evaluated by three healthcare providers, each of whom prescribed multiple courses of antibiotics and inhaled bronchodilators based on presumed diagnoses of bronchitis or COPD exacerbation. Notably, no chest imaging was performed at the initial stages. Chest imaging revealed left lung collapse, and bronchoscopy revealed a polypoidal mass obstructing the left main bronchus. Histopathological analysis confirmed the diagnosis of an endobronchial lipoma. This case highlights the importance of considering benign bronchial tumours in the differential diagnosis of chronic respiratory complaints, especially in patients with a smoking history. Complete excision, either bronchoscopic or surgical, is the treatment of choice, resulting in excellent prognosis and symptom resolution.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"13 7","pages":"e70291"},"PeriodicalIF":0.8,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12284315/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144700026","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Paraneoplastic Hypoglycaemia in a Patient With Solitary Fibrous Tumor of Pleura. 胸膜孤立性纤维性肿瘤伴副肿瘤性低血糖1例。
IF 0.8
Respirology Case Reports Pub Date : 2025-07-21 eCollection Date: 2025-07-01 DOI: 10.1002/rcr2.70275
Asmita A Mehta, Valiyaparambil Pavithran Praveen, Valathara Pradeep Lakshmi Priya, Liya Anil, Vishnu Nair
{"title":"Paraneoplastic Hypoglycaemia in a Patient With Solitary Fibrous Tumor of Pleura.","authors":"Asmita A Mehta, Valiyaparambil Pavithran Praveen, Valathara Pradeep Lakshmi Priya, Liya Anil, Vishnu Nair","doi":"10.1002/rcr2.70275","DOIUrl":"10.1002/rcr2.70275","url":null,"abstract":"<p><p>Solitary fibrous tumours (SFTs) are rare spindle cell neoplasms, predominantly benign, comprising less than 2% of all soft tissue masses. In rare cases, SFTs can lead to Doege-Potter syndrome, a paraneoplastic condition characterised by hypoglycaemia due to elevated levels of insulin-like growth factor II (IGF-II). Patients typically present with symptomatic hypoglycaemia related to this hormonal dysregulation. We report the case of a 70-year-old man who presented with weight loss, cough, fatigue, tingling, and episodes of confusion associated with recurrent hypoglycaemia. Chest radiography revealed a large soft tissue mass in the right lower hemithorax, and CT-guided biopsy confirmed tumour infiltration in the basal segment of the right lower lobe.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"13 7","pages":"e70275"},"PeriodicalIF":0.8,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12279444/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144691953","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Correction to "Evaluation of a Digital Health Model of Care for the Management of Adults With Symptomatic Malignant Pleural Effusion". 对“成人症状性恶性胸腔积液数字化健康护理模式评价”的修正。
IF 0.8
Respirology Case Reports Pub Date : 2025-07-18 eCollection Date: 2025-07-01 DOI: 10.1002/rcr2.70273
{"title":"Correction to \"Evaluation of a Digital Health Model of Care for the Management of Adults With Symptomatic Malignant Pleural Effusion\".","authors":"","doi":"10.1002/rcr2.70273","DOIUrl":"10.1002/rcr2.70273","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.1002/rcr2.70194.].</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"13 7","pages":"e70273"},"PeriodicalIF":0.8,"publicationDate":"2025-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12271973/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144676027","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Alveolar Sarcoidosis Mimicking Idiopathic Interstitial Pneumonia Without Mediastinal Lymphadenopathy. 肺泡结节病模拟特发性间质性肺炎,无纵隔淋巴结病。
IF 0.8
Respirology Case Reports Pub Date : 2025-07-16 eCollection Date: 2025-07-01 DOI: 10.1002/rcr2.70278
Hiroki Kanasaki, Noriyuki Enomoto, Yuko Tanaka, Suguru Kojima, Keisuke Morikawa, Shogo Nakai, Shusuke Yazawa, Yasutaka Mochizuka, Yusuke Inoue, Hideki Yasui, Hironao Hozumi, Yuzo Suzuki, Masato Karayama, Kazuki Furuhashi, Tomoyuki Fujisawa, Naoki Inui, Sayaka Ishigaki, Naro Ohashi, Yasunori Enomoto, Satoshi Baba, Kazuhiro Tabata, Takeshi Johkoh, Takafumi Suda
{"title":"Alveolar Sarcoidosis Mimicking Idiopathic Interstitial Pneumonia Without Mediastinal Lymphadenopathy.","authors":"Hiroki Kanasaki, Noriyuki Enomoto, Yuko Tanaka, Suguru Kojima, Keisuke Morikawa, Shogo Nakai, Shusuke Yazawa, Yasutaka Mochizuka, Yusuke Inoue, Hideki Yasui, Hironao Hozumi, Yuzo Suzuki, Masato Karayama, Kazuki Furuhashi, Tomoyuki Fujisawa, Naoki Inui, Sayaka Ishigaki, Naro Ohashi, Yasunori Enomoto, Satoshi Baba, Kazuhiro Tabata, Takeshi Johkoh, Takafumi Suda","doi":"10.1002/rcr2.70278","DOIUrl":"10.1002/rcr2.70278","url":null,"abstract":"<p><p>We present a case of alveolar sarcoidosis showing lower lobe-predominant areas of airspace consolidation and ground-glass attenuation on HRCT, mimicking idiopathic interstitial pneumonia (IIP) with spontaneous wandering. Mediastinal lymphadenopathy and uveitis were negative. Surgical lung biopsy revealed multiple non-necrotising granulomas. Alveolar sarcoidosis that mimics IIP without mediastinal lymphadenopathy is rare.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"13 7","pages":"e70278"},"PeriodicalIF":0.8,"publicationDate":"2025-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12266983/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144660642","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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