Respirology Case ReportsPub Date : 2026-09-16eCollection Date: 2026-09-01DOI: 10.1002/rcr2.70762
Toki Kitano, Yuki Takigawa, Ken Sato, Mayu Goda, Hitoshi Hara, Tomoya Osedo, Yuto Sasano, Keisuke Shiraha, Suzuka Matsuoka, Jun Nishimura, Hiromi Watanabe, Kenichiro Kudo, Keiichi Fujiwara
{"title":"Rescue Diagnosis of Upper-Lobar Station 12U Lymph Nodes Using the Thin Convex-Probe EBUS Bronchoscope (BF-UCP190F): A Report of Two Cases.","authors":"Toki Kitano, Yuki Takigawa, Ken Sato, Mayu Goda, Hitoshi Hara, Tomoya Osedo, Yuto Sasano, Keisuke Shiraha, Suzuka Matsuoka, Jun Nishimura, Hiromi Watanabe, Kenichiro Kudo, Keiichi Fujiwara","doi":"10.1002/rcr2.70762","DOIUrl":"https://doi.org/10.1002/rcr2.70762","url":null,"abstract":"<p><p>BF-UCP190F (Olympus) is a newly developed thin convex-probe endobronchial ultrasound (TCP-EBUS) bronchoscope, improving access to distal bronchi. We report two cases in which TCP-EBUS enabled successful endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) of the upper-lobar station 12U lymph node (#12U LN) via B<sup>3</sup> after conventional bronchoscopic forceps sampling failed to provide a definitive diagnosis. In the first case, forceps biopsy of a left upper lobe tumour was non-diagnostic; TCP-EBUS-guided EBUS-TBNA of the left #12U LN established lung adenocarcinoma with N1 involvement. In the second case, the initial bronchoscopy yielded only cytological evidence of carcinoma without histological confirmation; TCP-EBUS-guided sampling of the right #12U LN revealed metastatic small cell carcinoma. In both cases, the pathological diagnosis of EBUS-TBNA guided subsequent treatment. These cases suggest that BF-UCP190F expands the diagnostic range of bronchoscopy and may serve as a valuable rescue technique for sampling upper lobar hilar lymph nodes in clinical practice.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"14 9","pages":"e70762"},"PeriodicalIF":0.7,"publicationDate":"2026-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13581433/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148991768","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}
{"title":"Rapid Onset of Mesalazine-Induced Eosinophilic Pneumonia Manifesting 7 Days After Initiation: A Case Report.","authors":"Toshiaki Inazaki, Kenichiro Takeda, Mana Iwasaki, Hiroki Tajima, Yu Shionoya, Ryutaro Hirama, Shun Sato, Akira Naito, Takeshi Kawasaki, Jun Ikari, Satoko Kageyama, Jun-Ichiro Ikeda, Takuji Suzuki","doi":"10.1002/rcr2.70758","DOIUrl":"10.1002/rcr2.70758","url":null,"abstract":"<p><p>Mesalazine is a recognised cause of drug-induced eosinophilic pneumonia. The condition usually occurs after 2-6 months of therapy, and onset within the first week is rare. A 29-year-old woman with bronchial asthma and newly diagnosed ulcerative colitis was initiated on oral mesalazine. On Day 7, she developed a persistent cough. Three weeks later, imaging revealed a right upper-lobe pulmonary infiltrate, promoting referral for evaluation. Bronchoalveolar lavage and transbronchial cryobiopsy demonstrated marked eosinophilic infiltration, confirming eosinophilic pneumonia. Discontinuation of mesalazine led to rapid clinical and radiographic improvement. Clinical course and exclusion of alternative aetiologies identified mesalazine as the causative drug. This case demonstrates that mesalazine can induce eosinophilic pneumonia within 7 days of initiation.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"14 9","pages":"e70758"},"PeriodicalIF":0.7,"publicationDate":"2026-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13580153/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148991810","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}
{"title":"Bilateral Bloody Pleural Effusions With Discordant Cellular Patterns: A Case of Concurrent Parapneumonic Effusion and Dressler Syndrome.","authors":"Yoshitsugu Narumi, Susumu Hoshino, Midori Yamakawa, Yoshiko Amano","doi":"10.1002/rcr2.70764","DOIUrl":"https://doi.org/10.1002/rcr2.70764","url":null,"abstract":"<p><p>Bilateral pleural effusions typically suggest systemic aetiologies; however, concurrent distinct localised pathologies are rare. A 73-year-old man presented with fever and cough. Chest imaging revealed pneumonia and bilateral pleural effusions developed during antibiotic treatment. The right effusion was neutrophil-dominant, consistent with parapneumonic effusion, while the left was lymphocyte-dominant, suggesting Dressler syndrome triggered by pneumonia-induced systemic inflammation. Both effusions were bloody, an appearance possibly exacerbated by the concomitant use of a direct oral anticoagulant and aspirin. The left effusion recurred months later but significantly improved following ibuprofen treatment, supporting an immune-mediated aetiology. This case highlights that bilateral effusions can arise from different aetiologies and that pneumonia-induced inflammation may trigger a latent immune response related to prior cardiac surgery.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"14 9","pages":"e70764"},"PeriodicalIF":0.7,"publicationDate":"2026-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13580148/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148991851","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}
{"title":"Hot Tub Lung: Misdiagnosed Hypersensitivity Pneumonitis Revealing a Mycobacterial Aetiology-A Case Report and Literature Review.","authors":"Fadi Abualhommos, Rahaf Fetyani, Yasmeen Butt, Michael Gotway, Abeer Almajali, Jehad Azar","doi":"10.1002/rcr2.70741","DOIUrl":"10.1002/rcr2.70741","url":null,"abstract":"<p><p>Hot tub lung (HTL) is a rare granulomatous pneumonitis caused by inhalational exposure to <i>Mycobacterium avium</i> complex (MAC)-contaminated hot tub water, with debated pathogenesis encompassing both hypersensitivity and infectious mechanisms. A 66-year-old woman with progressive exertional dyspnea was initially misdiagnosed with non-fibrotic hypersensitivity pneumonitis attributed to pheasant exposure and treated with corticosteroids and mycophenolate without improvement. High-resolution CT demonstrated diffuse centrilobular nodules with air-trapping. Surgical lung biopsy revealed bronchiolocentric non-necrotizing granulomas with rare MAC organisms despite negative bronchoalveolar lavage cultures. Detailed clinical history disclosed daily indoor hot tub use coinciding with symptom onset. Following hot tub cessation and initiation of azithromycin, ethambutol and rifabutin, she ultimately achieved complete clinical and radiologic resolution. HTL represents a heterogeneous spectrum from immune-mediated hypersensitivity to true mycobacterial infection. Persistent interstitial lung disease despite ongoing immunosuppression should prompt a thorough hot tub exposure history and selected patients may require antimycobacterial therapy alongside exposure cessation.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"14 9","pages":"e70741"},"PeriodicalIF":0.7,"publicationDate":"2026-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13575854/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148978217","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}
Respirology Case ReportsPub Date : 2026-09-15eCollection Date: 2026-09-01DOI: 10.1002/rcr2.70761
Gerardo Arwi, Adriana Avram, Philip Bardin
{"title":"Recurrent Asthma Exacerbations Secondary to Gastric Stenosis After Gastric Band Slippage: Case Report and Literature Review.","authors":"Gerardo Arwi, Adriana Avram, Philip Bardin","doi":"10.1002/rcr2.70761","DOIUrl":"https://doi.org/10.1002/rcr2.70761","url":null,"abstract":"<p><p>Recurrent asthma exacerbations despite optimal therapy warrant investigation for alternative causes. In this setting, silent aspiration is a key but often forgotten trigger of airway inflammation that should be considered in the differential diagnosis. We present a patient with long-standing severe Type 2 asthma complicated by recurrent exacerbations of an infective nature that was ultimately found to be associated with gastric band slippage causing gastric stenosis and delayed gastric emptying. Exacerbations ceased after surgical intervention and removal of the band. The report highlights the importance of considering gastrointestinal causes, particularly in people with prior gastric surgery, as a reason for poor asthma control and repeat exacerbations. We review literature pertaining to this field and emphasise the need for a multidisciplinary approach (including surgical intervention) to identify and effectively treat silent aspiration.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"14 9","pages":"e70761"},"PeriodicalIF":0.7,"publicationDate":"2026-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13578907/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148991860","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}
{"title":"Pulmonary Amyloidosis Diagnosed by Transbronchial Lung Biopsy: A Three-Case Series With Diverse Radiological Manifestations.","authors":"Masaki Tanaka, Yuri Ozaki, Takuo Otsuka, Takahide Hongo, Mari Tone, Yuhei Kinehara, Shoichi Ihara, Yoshito Takeda, Ryu Jokoji, Isao Tachibana","doi":"10.1002/rcr2.70757","DOIUrl":"https://doi.org/10.1002/rcr2.70757","url":null,"abstract":"<p><p>Pulmonary amyloidosis is a rare disease with diverse radiological manifestations that may mimic malignancy or diffuse interstitial lung disease. Although conventional forceps transbronchial lung biopsy (TBLB) is an established less invasive diagnostic method, its clinical role may differ according to disease presentation. We report three patients with pulmonary amyloidosis diagnosed by conventional forceps TBLB. Two presented with nodular lesions mimicking malignancy; TBLB established the diagnosis, and systemic evaluation showed no extrapulmonary involvement, supporting localized pulmonary amyloidosis. The third presented with progressive weight loss and diffuse interlobular septal thickening. TBLB unexpectedly demonstrated pulmonary amyloid deposition, prompting systemic and haematological evaluation that revealed systemic AL amyloidosis associated with multiple myeloma. These cases illustrate distinct roles of conventional forceps TBLB: distinguishing localized nodular amyloidosis from malignancy and, in diffuse alveolar-septal disease, providing an initial clue prompting evaluation for systemic amyloidosis.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"14 9","pages":"e70757"},"PeriodicalIF":0.7,"publicationDate":"2026-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13578924/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148991790","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}
Respirology Case ReportsPub Date : 2026-09-15eCollection Date: 2026-09-01DOI: 10.1002/rcr2.70755
Xiaerbate Zakeerjiang, Yu ChenYi, Liu Bing, Liu Bin, Liu YaTing, Yuan YiFei
{"title":"Individualized Stent for Tracheal Fistula Complicating Tracheostomy Following Esophagectomy.","authors":"Xiaerbate Zakeerjiang, Yu ChenYi, Liu Bing, Liu Bin, Liu YaTing, Yuan YiFei","doi":"10.1002/rcr2.70755","DOIUrl":"10.1002/rcr2.70755","url":null,"abstract":"<p><p>Delayed-onset tracheal fistula following esophagectomy with concurrent tracheostomy is rare and poses diagnostic challenges. A 79-year-old female patient with oesophageal squamous cell carcinoma (ESCC) developed a tracheal fistula following esophagectomy and tracheostomy. Repeated bronchoscopies via the tracheostoma failed to visualize the fistula orifice; the diagnosis was confirmed by computed tomography (CT) with oral contrast medium and complete tracheal inspection following temporary removal of the tracheostomy tube. A patient-specific, fully covered self-expandable metallic stent (FCSEMS) was implanted under endoscopic guidance. At 53 days of follow-up, the stent remained well-positioned without aspiration recurrence. The patient ultimately succumbed to distant tumour metastasis and multidrug-resistant bacterial infection. Complete tracheobronchoscopy following temporary decannulation and CT with oral contrast medium facilitates the diagnosis of tracheal fistula. Individualized covered stenting achieves satisfactory fistula occlusion, thereby providing valuable clinical insights for the management of similar complex cases.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"14 9","pages":"e70755"},"PeriodicalIF":0.7,"publicationDate":"2026-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13575761/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148978171","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}
Respirology Case ReportsPub Date : 2026-09-08eCollection Date: 2026-09-01DOI: 10.1002/rcr2.70703
Chia-Ni Liu, Hsiao-Chin Shen, Yi-Chen Yeh
{"title":"An Underrecognized Cause of Recurrent Spontaneous Pneumothorax: Birt-Hogg-Dubé Syndrome With Isolated Pulmonary Manifestation.","authors":"Chia-Ni Liu, Hsiao-Chin Shen, Yi-Chen Yeh","doi":"10.1002/rcr2.70703","DOIUrl":"10.1002/rcr2.70703","url":null,"abstract":"<p><p>Birt-Hogg-Dubé (BHD) syndrome is a rare autosomal dominant disorder characterized by a classic triad of cutaneous fibrofolliculomas, bilateral pulmonary cysts and renal tumours. Pulmonary manifestations may occur in isolation, posing a significant diagnostic challenge. We report a 50-year-old non-smoking woman with recurrent pneumothorax referred to our pulmonology clinic for dyspnoea on exertion. Chest CT revealed multiple bilateral pulmonary cysts with lower-lobe predominance. Review of prior wedge resection specimens showed subpleural and parenchymal cysts lined by flattened epithelium. Negative immunohistochemical staining for HMB-45 and GPNMB excluded lymphangioleiomyomatosis. Given the characteristic cyst pattern, germline whole-exome sequencing identified a pathogenic heterozygous FLCN frameshift variant, confirming the diagnosis. Because of the lifetime risk of renal malignancy, early recognition is important and genetic testing is recommended when BHD is suspected.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"14 9","pages":"e70703"},"PeriodicalIF":0.7,"publicationDate":"2026-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13554708/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148920373","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}
Respirology Case ReportsPub Date : 2026-09-08eCollection Date: 2026-09-01DOI: 10.1002/rcr2.70702
Rahaf A Jereisat, Nawras Ibrahim, Maher Dahdel
{"title":"Disease-Intrinsic Organising Pneumonia During Biomarker-Confirmed Ulcerative Colitis Remission.","authors":"Rahaf A Jereisat, Nawras Ibrahim, Maher Dahdel","doi":"10.1002/rcr2.70702","DOIUrl":"10.1002/rcr2.70702","url":null,"abstract":"<p><p>Organising pneumonia is an increasingly recognised pulmonary manifestation of ulcerative colitis, though nearly all reported cases are attributed to drug-induced aetiology. The 2025 ERS/ATS classification of interstitial pneumonias now explicitly lists ulcerative colitis among secondary causes of cicatricial organising pneumonia, formally recognising a disease-intrinsic mechanism for organising pneumonia in ulcerative colitis. We present a 76-year-old woman with 10-year ulcerative colitis pancolitis on stable mesalamine in biochemical remission (faecal calprotectin 62 μg/g, below the 80 μg/g histological activity threshold) who developed progressive dyspnea. Drug-induced aetiology was systematically excluded: mesalamine had been stable for 10 years, discontinuation produced no improvement, and corticosteroids were required for response. Transbronchial cryobiopsy was initially interpreted as fibrotic non-specific interstitial pneumonia; expert pathology consultation revised the diagnosis to organising pneumonia with Masson bodies, changing management from antifibrotics to corticosteroids, illustrating the clinical consequences of cryobiopsy diagnostic discordance. Bronchoalveolar lavage revealed a neutrophil-predominant profile (42% neutrophils, 3% lymphocytes), atypical for cryptogenic organising pneumonia, which typically shows lymphocytic predominance. This pattern may reflect gut-lung axis immune trafficking in secondary organising pneumonia associated with ulcerative colitis. Concurrent seronegative arthritis was reclassified as ulcerative colitis-associated spondyloarthropathy, removing rheumatoid arthritis-associated interstitial lung disease from the differential. This case extends the sole prior report of organising pneumonia during confirmed ulcerative colitis remission by incorporating biomarker-confirmed remission, systematic drug exclusion, cryobiopsy discordance with treatment-altering consequences and contextualisation within the updated 2025 ERS/ATS classification framework.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"14 9","pages":"e70702"},"PeriodicalIF":0.7,"publicationDate":"2026-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13554710/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148920423","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}
{"title":"Congenital Bronchial Atresia Mimicking Pulmonary Sequestration in the Lower Lobe: A Case Report.","authors":"Shohei Mitsumata, Kensuke Midorikawa, Kentaro Wakamatsu, Shiro Kaneda, Takuro Futamata, Tsuyoshi Iwanaka, Yuichiro Ueda, So Miyahara, Yoshiko Masuda, Hiroyasu Nakashima, Toshihiko Sato","doi":"10.1002/rcr2.70712","DOIUrl":"10.1002/rcr2.70712","url":null,"abstract":"<p><p>Congenital bronchial atresia (CBA) is a rare airway anomaly that may radiologically resemble other congenital pulmonary lesions, particularly when it occurs in the lower lobes. A 41-year-old woman was referred for surgical treatment of suspected pulmonary sequestration based on imaging findings. Computed tomography (CT) at the referring hospital showed a cavitary lesion with fluid retention in Segment 7 (S7) of the right lower lobe, with surrounding ground-glass opacity, suggesting infection associated with pulmonary sequestration. Re-evaluation at our institution identified the lesion as a bronchocele with focal hyperinflation, interruption of the segmental bronchus (B7), and a normally distributed pulmonary artery (A7) without aberrant systemic supply. Three-dimensional CT clearly demonstrated these bronchovascular features and supported the diagnosis of CBA. Thoracoscopic right lower lobectomy was performed, and histopathological findings confirmed the diagnosis of CBA. This case highlights the importance of systematic evaluation of bronchial continuity and vascular supply in congenital lower-lobe lesions, for which three-dimensional CT reconstruction may be useful.</p>","PeriodicalId":45846,"journal":{"name":"Respirology Case Reports","volume":"14 9","pages":"e70712"},"PeriodicalIF":0.7,"publicationDate":"2026-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13551000/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148913469","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}