Semin Respir Crit Care Med
DOI: 10.1055/a-2716-1746
Review Article

Malignancies Presenting with Alveolar Infiltrates: Diagnostic Pitfalls, Radiologic Clues, and Clinical Patterns

Authors

  • Akshay Mathavan

    1   Department of Internal Medicine, University of Florida, Gainesville, Florida, United States
  • Akash Mathavan

    1   Department of Internal Medicine, University of Florida, Gainesville, Florida, United States
  • Olga R. G. Rojas

    2   Division of Pulmonary, Critical Care, and Sleep Medicine, University of Florida, Gainesville, Florida, United States
  • Ali Ataya

    2   Division of Pulmonary, Critical Care, and Sleep Medicine, University of Florida, Gainesville, Florida, United States
Preview

Abstract

Alveolar infiltrates are a common but nonspecific radiologic finding that can obscure the diagnosis of underlying malignancy. While infections and inflammatory processes are typical considerations, a subset of cancers, both primary and secondary, can present with alveolar opacities that mimic these benign conditions. This review synthesizes the spectrum of neoplastic diseases that manifest with an alveolar radiographic pattern, focusing on both primary pulmonary malignancies (such as lepidic-predominant adenocarcinoma, invasive mucinous adenocarcinoma, and pulmonary lymphoma) and select metastatic solid tumors (notably renal cell carcinoma, gastrointestinal cancers, melanoma, and breast cancer) that exhibit a nondestructive, airspace-filling growth. We also describe secondary and paraneoplastic processes, including immune-mediated pneumonitis, eosinophilic pneumonia, leukemic pulmonary hemorrhage, diffuse alveolar hemorrhage, and secondary alveolar proteinosis, that can similarly produce alveolar opacities in the setting of malignancy. Each entity is discussed with emphasis on its clinical presentation, diagnostic approach, imaging features, and distinguishing characteristics. Radiographic findings and other diagnostics are integrated to highlight the importance of early recognition and appropriate investigation. Distinguishing malignant from infectious or inflammatory causes of alveolar disease remains challenging but critical, as misdiagnosis can lead to inappropriate treatment or delays in therapy. Summary tables are provided to support practical clinical differentiation and management. By improving recognition of neoplastic causes of alveolar infiltrates, clinicians may better tailor diagnostic workups and initiate appropriate treatment strategies.

Contributors' Statement

Akshay M. was the primary author who synthesized relevant information and drafted the manuscript. All other authors assisted in drafting portions of the text and provided critical revision. A.A. is responsible for the final version of the manuscript.




Publikationsverlauf

Eingereicht: 15. Juli 2025

Angenommen: 02. Oktober 2025

Accepted Manuscript online:
06. Oktober 2025

Artikel online veröffentlicht:
17. Oktober 2025

© 2025. Thieme. All rights reserved.

Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA

 
  • References

  • 1 Ost DE, Jim Yeung S-C, Tanoue LT, Gould MK. Clinical and organizational factors in the initial evaluation of patients with lung cancer: diagnosis and management of lung cancer, 3rd ed: American College of Chest Physicians evidence-based clinical practice guidelines. Chest 2013; 143 (5 suppl): e121S-e141S
  • 2 Snoeckx A, Dendooven A, Carp L. et al. Wolf in sheep's clothing: primary lung cancer mimicking benign entities. Lung Cancer 2017; 112: 109-117
  • 3 Wingard JR, Hiemenz JW, Jantz MA. How I manage pulmonary nodular lesions and nodular infiltrates in patients with hematologic malignancies or undergoing hematopoietic cell transplantation. Blood 2012; 120 (09) 1791-1800
  • 4 Yao D, Zhang L, Wu PL. et al. Clinical and misdiagnosed analysis of primary pulmonary lymphoma: a retrospective study. BMC Cancer 2018; 18 (01) 281
  • 5 Zhang S, Yu X, Huang Y. et al. Pneumonic-type invasive mucinous adenocarcinoma and infectious pneumonia: clinical and CT imaging analysis from multiple centers. BMC Pulm Med 2022; 22 (01) 460
  • 6 Singh H, Hirani K, Kadiyala H. et al. Characteristics and predictors of missed opportunities in lung cancer diagnosis: an electronic health record-based study. J Clin Oncol 2010; 28 (20) 3307-3315
  • 7 Yoo H, Suh GY, Jeong B-H. et al. Etiologies, diagnostic strategies, and outcomes of diffuse pulmonary infiltrates causing acute respiratory failure in cancer patients: a retrospective observational study. Crit Care 2013; 17 (04) R150
  • 8 Schwartz AM, Rezaei MK. Diagnostic surgical pathology in lung cancer: Diagnosis and management of lung cancer, 3rd ed: American College of Chest Physicians evidence-based clinical practice guidelines. Chest 2013; 143 (05) e251S-e262S
  • 9 Travis WD, Brambilla E, Noguchi M. et al. Diagnosis of lung adenocarcinoma in resected specimens: implications of the 2011 International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society classification. Arch Pathol Lab Med 2013; 137 (05) 685-705
  • 10 Travis WD, Brambilla E, Noguchi M. et al. International association for the study of lung cancer/American Thoracic Society/European Respiratory Society international multidisciplinary classification of lung adenocarcinoma. J Thorac Oncol 2011; 6 (02) 244-285
  • 11 Kadota K, Villena-Vargas J, Yoshizawa A. et al. Prognostic significance of adenocarcinoma in situ, minimally invasive adenocarcinoma, and nonmucinous lepidic predominant invasive adenocarcinoma of the lung in patients with stage I disease. Am J Surg Pathol 2014; 38 (04) 448-460
  • 12 Weichert W, Warth A. Early lung cancer with lepidic pattern: adenocarcinoma in situ, minimally invasive adenocarcinoma, and lepidic predominant adenocarcinoma. Curr Opin Pulm Med 2014; 20 (04) 309-316
  • 13 Pittaro A, Crivelli F, Orlando G. et al. Pulmonary low malignant potential adenocarcinoma: a validation of the proposed criteria for this novel subtype. Am J Surg Pathol 2024; 48 (02) 204-211
  • 14 Yambayev I, Sullivan TB, Suzuki K. et al. Pulmonary adenocarcinomas of low malignant potential: proposed criteria to expand the spectrum beyond adenocarcinoma in situ and minimally invasive adenocarcinoma. Am J Surg Pathol 2021; 45 (04) 567-576
  • 15 Moghaddam SJ, Savai R, Salehi-Rad R. et al. Premalignant progression in the lung: knowledge gaps and novel opportunities for interception of non-small cell lung cancer. An Official American Thoracic Society Research Statement. Am J Respir Crit Care Med 2024; 210 (05) 548-571
  • 16 Naito M, Aokage K, Saruwatari K. et al. Microenvironmental changes in the progression from adenocarcinoma in situ to minimally invasive adenocarcinoma and invasive lepidic predominant adenocarcinoma of the lung. Lung Cancer 2016; 100: 53-62
  • 17 Juul NH, Yoon J-K, Martinez MC. et al. KRAS(G12D) drives lepidic adenocarcinoma through stem-cell reprogramming. Nature 2023; 619 (7971) 860-867
  • 18 Austin JHM, Garg K, Aberle D. et al. Radiologic implications of the 2011 classification of adenocarcinoma of the lung. Radiology 2013; 266 (01) 62-71
  • 19 Chang WC, Zhang YZ, Nicholson AG. Pulmonary invasive mucinous adenocarcinoma. Histopathology 2024; 84 (01) 18-31
  • 20 Kim HS, Dugan AJ, Godden J, Chao CY, Chae YK. Clinicopathologic and molecular landscape of invasive mucinous adenocarcinoma of the lung. J Clin Oncol 2024; 42 (16) 8037-8037
  • 21 Boland JM, Maleszewski JJ, Wampfler JA. et al. Pulmonary invasive mucinous adenocarcinoma and mixed invasive mucinous/nonmucinous adenocarcinoma-a clinicopathological and molecular genetic study with survival analysis. Hum Pathol 2018; 71: 8-19
  • 22 Aimalla N, Kesireddy M, Yadukumar L. Incidence trends and factors affecting survival in mucinous adenocarcinoma of the lung: insights from SEER data. J Clin Oncol 2024; 42 (16) e20090-e20090
  • 23 Ueda D, Ito M, Tsutani Y. et al. Comprehensive analysis of the clinicopathological features, targetable profile, and prognosis of mucinous adenocarcinoma of the lung. J Cancer Res Clin Oncol 2021; 147 (12) 3709-3718
  • 24 Kishikawa S, Hayashi T, Saito T. et al. Diffuse expression of MUC6 defines a distinct clinicopathological subset of pulmonary invasive mucinous adenocarcinoma. Mod Pathol 2021; 34 (04) 786-797
  • 25 Kadota K, Yeh Y-C, D'Angelo SP. et al. Associations between mutations and histologic patterns of mucin in lung adenocarcinoma: invasive mucinous pattern and extracellular mucin are associated with KRAS mutation. Am J Surg Pathol 2014; 38 (08) 1118-1127
  • 26 Sugano M, Nagasaka T, Sasaki E. et al. HNF4α as a marker for invasive mucinous adenocarcinoma of the lung. Am J Surg Pathol 2013; 37 (02) 211-218
  • 27 Sun X, Zeng B, Tan X, Chen Z, Pan X, Jiang L. Invasive mucinous adenocarcinoma of the lung: clinicopathological features, 18F-FDG PET/CT findings, and survival outcomes. Ann Nucl Med 2023; 37 (03) 198-207
  • 28 Miyamoto A, Kurosaki A, Fujii T, Kishi K, Homma S. HRCT features of surgically resected invasive mucinous adenocarcinoma associated with interstitial pneumonia. Respirology 2017; 22 (04) 735-743
  • 29 Detterbeck FC, Lewis SZ, Diekemper R, Addrizzo-Harris D, Alberts WM. Executive summary: diagnosis and management of lung cancer, 3rd ed: American College of Chest Physicians evidence-based clinical practice guidelines. Chest 2013; 143 (05) 7S-37S
  • 30 Rivera MP, Mehta AC, Wahidi MM. Establishing the diagnosis of lung cancer: diagnosis and management of lung cancer, 3rd ed: American College of Chest Physicians evidence-based clinical practice guidelines. Chest 2013; 143 (05) e142S-e165S
  • 31 Kidane B, Bott M, Spicer J. et al; Expert Consensus Panel. The American Association for Thoracic Surgery (AATS) 2023 Expert Consensus Document: staging and multidisciplinary management of patients with early-stage non-small cell lung cancer. J Thorac Cardiovasc Surg 2023; 166 (03) 637-654
  • 32 Shen F, Wu X, Geng J, Guo W, Duan J. Prognostic factors for resected invasive mucinous lung adenocarcinoma: a systematic review and meta-analysis. BMC Cancer 2024; 24 (01) 1317
  • 33 Lee JO, Lee GD, Choi S. et al. Surgical prognosis of lung invasive mucinous and non-mucinous adenocarcinoma: propensity score matched analysis. Eur J Cardiothorac Surg 2024; 66 (03) ezae316
  • 34 Lee HY, Cha MJ, Lee KS. et al. Prognosis in resected invasive mucinous adenocarcinomas of the lung: related factors and comparison with resected nonmucinous adenocarcinomas. J Thorac Oncol 2016; 11 (07) 1064-1073
  • 35 Saito T, Tsuta K, Honda O. et al. Prognostic impact of mucin spread, tumor cell spread, and invasive size in invasive mucinous adenocarcinoma of the lung. Lung Cancer 2020; 146: 50-57
  • 36 Li W, Yang Y, Yang M. et al. Clinicopathologic features and survival outcomes of primary lung mucinous adenocarcinoma based on different radiologic subtypes. Ann Surg Oncol 2024; 31 (01) 167-177
  • 37 Kris MG, Gaspar LE, Chaft JE. et al. Adjuvant systemic therapy and adjuvant radiation therapy for stage I to IIIA completely resected non-small-cell lung cancers: American Society of Clinical Oncology/Cancer Care Ontario Clinical Practice Guideline Update. J Clin Oncol 2017; 35 (25) 2960-2974
  • 38 Zhang Y-N, Cao K, Yang Y. et al. Case report: do not diagnose lung cancer as pneumonia: continue to monitor a case of invasive mucinous adenocarcinoma as it progresses from small to large. Front Med (Lausanne) 2025; 12: 1578874
  • 39 Zhu D, Zhang Q, Rui Z, Xu S. Pulmonary invasive mucinous adenocarcinoma mimicking pulmonary actinomycosis. BMC Pulm Med 2022; 22 (01) 181
  • 40 Sanguedolce F, Zanelli M, Zizzo M. et al. Primary pulmonary B-cell lymphoma: a review and update. Cancers (Basel) 2021; 13 (03) 415
  • 41 Borie R, Wislez M, Antoine M, Cadranel J. Lymphoproliferative disorders of the lung. Respiration 2017; 94 (02) 157-175
  • 42 Piña-Oviedo S, Weissferdt A, Kalhor N, Moran CA. Primary pulmonary lymphomas. Adv Anat Pathol 2015; 22 (06) 355-375
  • 43 Wang Y, Han J, Zhang F. et al. Comparison of radiologic characteristics and pathological presentations of primary pulmonary lymphoma in 22 patients. J Int Med Res 2020; 48 (04) 300060519879854
  • 44 He H, Tan F, Xue Q. et al. Clinicopathological characteristics and prognostic factors of primary pulmonary lymphoma. J Thorac Dis 2021; 13 (02) 1106-1117
  • 45 Hu M, Gu W, Chen S, Mei J, Wang W. Clinical analysis of 50 cases of primary pulmonary lymphoma: a retrospective study and literature review. Technol Cancer Res Treat 2022 21 :15330338221075529
  • 46 Vela V, Juskevicius D, Prince SS. et al. Deciphering the genetic landscape of pulmonary lymphomas. Mod Pathol 2021; 34 (02) 371-379
  • 47 Shen H, Zhou Y. Clinical features and surgical treatment of primary pulmonary lymphoma: a retrospective study. Front Oncol 2022; 12: 779395
  • 48 Deng W, Wan Y, Yu JQ. Pulmonary MALT Lymphoma has variable features on CT. Sci Rep 2019; 9 (01) 8657
  • 49 Bi W, Zhao S, Wu C. et al. Pulmonary mucosa-associated lymphoid tissue lymphoma: CT findings and pathological basis. J Surg Oncol 2021; 123 (05) 1336-1344
  • 50 Li S, Wang L, Chang N. et al. Differential clinical and CT imaging features of pneumonic-type primary pulmonary lymphoma and pneumonia: a retrospective multicentre observational study. BMJ Open 2023; 13 (10) e077198
  • 51 Chen Y, Chen A, Jiang H. et al. HRCT in primary pulmonary lymphoma: can CT imaging phenotypes differentiate histological subtypes between mucosa-associated lymphoid tissue (MALT) lymphoma and non-MALT lymphoma?. J Thorac Dis 2018; 10 (11) 6040-6049
  • 52 Ooi GC, Chim CS, Lie AKW, Tsang KWT. Computed tomography features of primary pulmonary non-Hodgkin's lymphoma. Clin Radiol 1999; 54 (07) 438-443
  • 53 Cadranel J, Wislez M, Antoine M. Primary pulmonary lymphoma. Eur Respir J 2002; 20 (03) 750-762
  • 54 Lin H, Zhou K, Peng Z, Liang L, Cao J, Mei J. Surgery and chemotherapy cannot improve the survival of patients with early-stage mucosa-associated lymphoid tissue derived primary pulmonary lymphoma. Front Oncol 2022; 12: 965727
  • 55 Berkman N, Breuer R, Kramer MR, Polliack A. Pulmonary involvement in lymphoma. Leuk Lymphoma 1996; 20 (3–4): 229-237
  • 56 Pan Z, Xu ML. T-cell and NK-cell lymphomas in the lung. Semin Diagn Pathol 2020; 37 (06) 273-282
  • 57 Hare SS, Souza CA, Bain G. et al. The radiological spectrum of pulmonary lymphoproliferative disease. Br J Radiol 2012; 85 (1015) 848-864
  • 58 Eisner MD, Kaplan LD, Herndier B, Stulbarg MS. The pulmonary manifestations of AIDS-related non-Hodgkin's lymphoma. Chest 1996; 110 (03) 729-736
  • 59 Costa MBG, Siqueira SAC, Saldiva PHN, Rabe KF, Mauad T. Histologic patterns of lung infiltration of B-cell, T-cell, and Hodgkin lymphomas. Am J Clin Pathol 2004; 121 (05) 718-726
  • 60 Balikian JP, Herman PG. Non-Hodgkin lymphoma of the lungs. Radiology 1979; 132 (03) 569-576
  • 61 Fujita N, Ando M, Goto A. et al. Diffuse large B-cell lymphoma arising from the lesion of chronic lobar atelectasis. Tohoku J Exp Med 2020; 250 (02) 129-135
  • 62 Wang S, Zheng Y, Wang Z. et al. Comparison of chest CT manifestations of coronavirus disease 2019 (COVID-19) and pneumonia associated with lymphoma. Int J Med Sci 2020; 17 (13) 1909-1915
  • 63 Zompi S, Couderc L-J, Cadranel J. et al. Clonality analysis of alveolar B lymphocytes contributes to the diagnostic strategy in clinical suspicion of pulmonary lymphoma. Blood 2004; 103 (08) 3208-3215
  • 64 Cheson BD, Fisher RI, Barrington SF. et al; Alliance, Australasian Leukaemia and Lymphoma Group, Eastern Cooperative Oncology Group, European Mantle Cell Lymphoma Consortium, Italian Lymphoma Foundation, European Organisation for Research, Treatment of Cancer/Dutch Hemato-Oncology Group, Grupo Español de Médula Ósea, German High-Grade Lymphoma Study Group, German Hodgkin's Study Group, Japanese Lymphorra Study Group, Lymphoma Study Association, NCIC Clinical Trials Group, Nordic Lymphoma Study Group, Southwest Oncology Group, United Kingdom National Cancer Research Institute. Recommendations for initial evaluation, staging, and response assessment of Hodgkin and non-Hodgkin lymphoma: the Lugano classification. J Clin Oncol 2014; 32 (27) 3059-3068
  • 65 Marchesi F, Cattaneo C, Criscuolo M. et al; Sorveglianza Epidemiologica Infezioni nelle Emopatie (SEIFEM) Group. A bronchoalveolar lavage-driven antimicrobial treatment improves survival in hematologic malignancy patients with detected lung infiltrates: a prospective multicenter study of the SEIFEM group. Am J Hematol 2019; 94 (10) 1104-1112
  • 66 Koh TT, Colby TV, Müller NL. Myeloid leukemias and lung involvement. Semin Respir Crit Care Med 2005; 26 (05) 514-519
  • 67 Kakihana K, Ohashi K, Sakai F. et al. Leukemic infiltration of the lung following allogeneic hematopoietic stem cell transplantation. Int J Hematol 2009; 89 (01) 118-122
  • 68 Hill BT, Weil AC, Kalaycio M, Cook JR. Pulmonary involvement by chronic lymphocytic leukemia/small lymphocytic lymphoma is a specific pathologic finding independent of inflammatory infiltration. Leuk Lymphoma 2012; 53 (04) 589-595
  • 69 Shroff GS, Truong MT, Carter BW. et al. Leukemic involvement in the thorax. Radiographics 2019; 39 (01) 44-61
  • 70 Khoury JD, Chen W. Myeloid diseases in the lung and pleura. Semin Diagn Pathol 2020; 37 (06) 296-302
  • 71 Wu Y-K, Huang Y-C, Huang S-F, Huang C-C, Tsai Y-H. Acute respiratory distress syndrome caused by leukemic infiltration of the lung. J Formos Med Assoc 2008; 107 (05) 419-423
  • 72 Tanaka N, Matsumoto T, Miura G. et al. CT findings of leukemic pulmonary infiltration with pathologic correlation. Eur Radiol 2002; 12 (01) 166-174
  • 73 Stefanski M, Jamis-Dow C, Bayerl M, Desai RJ, Claxton DF, Van de Louw A. Chest radiographic and CT findings in hyperleukocytic acute myeloid leukemia: a retrospective cohort study of 73 patients. Medicine (Baltimore) 2016; 95 (44) e5285
  • 74 Potenza L, Luppi M, Morselli M. et al. Leukaemic pulmonary infiltrates in adult acute myeloid leukaemia: a high-resolution computerized tomography study. Br J Haematol 2003; 120 (06) 1058-1061
  • 75 O'Leary M, Cantley RL, Kluskens L, Gattuso P. Cytologic findings of acute leukemia in bronchoalveolar lavage fluid. Diagn Cytopathol 2013; 41 (07) 613-616
  • 76 Maschmeyer G, Donnelly JP. How to manage lung infiltrates in adults suffering from haematological malignancies outside allogeneic haematopoietic stem cell transplantation. Br J Haematol 2016; 173 (02) 179-189
  • 77 Leis JF, Primack SL, Schubach SE, Curtin PT, Druker BJ, Maziarz RT. Management of life-threatening pulmonary leukostasis with single agent imatinib mesylate during CML myeloid blast crisis. Haematologica 2004; 89 (09) ECR30
  • 78 ZuWallack RL, Urman JD, Lahiri B. Metastatic melanoma. Another cause of a solitary pulmonary nodule with an air bronchogram. Radiology 1977; 123 (02) 286-286
  • 79 Gaeta M, Volta S, Scribano E, Loria G, Vallone A, Pandolfo I. Air-space pattern in lung metastasis from adenocarcinoma of the GI tract. J Comput Assist Tomogr 1996; 20 (02) 300-304
  • 80 Seo JB, Im JG, Goo JM, Chung MJ, Kim MY. Atypical pulmonary metastases: spectrum of radiologic findings. Radiographics 2001; 21 (02) 403-417
  • 81 Webb WR, Gamsu G. Thoracic metastasis in malignant melanoma. A radiographic survey of 65 patients. Chest 1977; 71 (02) 176-181
  • 82 Wei H, Miao J, Cui J. et al. The prognosis and clinicopathological features of different distant metastases patterns in renal cell carcinoma: analysis based on the SEER database. Sci Rep 2021; 11 (01) 17822
  • 83 Xue J, Chen W, Xu W. et al. Patterns of distant metastases in patients with clear cell renal cell carcinoma–a population-based analysis. Cancer Med 2021; 10 (01) 173-187
  • 84 Dudani S, de Velasco G, Wells JC. et al. Evaluation of clear cell, papillary, and chromophobe renal cell carcinoma metastasis sites and association with survival. JAMA Netw Open 2021; 4 (01) e2021869
  • 85 Krishnan V, Bane SM, Kawle PD, Naresh KN, Kalraiya RD. Altered melanoma cell surface glycosylation mediates organ specific adhesion and metastasis via lectin receptors on the lung vascular endothelium. Clin Exp Metastasis 2005; 22 (01) 11-24
  • 86 Akhtar M, Haider A, Rashid S, Al-Nabet ADMH. Paget's “seed and soil” theory of cancer metastasis: an idea whose time has come. Adv Anat Pathol 2019; 26 (01) 69-74
  • 87 Xiong K, Qi M, Stoeger T, Zhang J, Chen S. The role of tumor-associated macrophages and soluble mediators in pulmonary metastatic melanoma. Front Immunol 2022; 13: 1000927
  • 88 Padua D, Zhang XH-F, Wang Q. et al. TGFbeta primes breast tumors for lung metastasis seeding through angiopoietin-like 4. Cell 2008; 133 (01) 66-77
  • 89 Franquet T, Rosado-de-Christenson ML, Marchiori E, Abbott GF, Martínez-Jiménez S, López L. Uncommon thoracic manifestations from extrapulmonary tumors: computed tomography evaluation - pictorial review. Respir Med 2020; 168: 105986
  • 90 Meacci E, Nachira D, Congedo MT. et al. Surgical resection of pulmonary metastases from melanoma in oligometastatic patients: results from a multicentric study in the era of immunoncology and targeted therapy. Cancers (Basel) 2023; 15 (09) 2462
  • 91 Baldes N, Eberlein M, Bölükbas S. Multimodal and palliative treatment of patients with pulmonary metastases. J Thorac Dis 2021; 13 (04) 2686-2691
  • 92 Manucha V, Hansen JT, Gonzalez MF, Akhtar I. Role of cytology and immunochemistry in diagnosis of metastatic malignancies in the lung: a critical appraisal. Diagn Cytopathol 2018; 46 (11) 936-944
  • 93 Libshitz HI, Baber CE, Hammond CB. The pulmonary metastases of choriocarcinoma. Obstet Gynecol 1977; 49 (04) 412-416
  • 94 Kelly MP, Rustin GJS, Ivory C, Phillips P, Bagshawe KD. Respiratory failure due to choriocarcinoma: a study of 103 dyspneic patients. Gynecol Oncol 1990; 38 (02) 149-154
  • 95 Rejlekova K, Cursano MC, De Giorgi U, Mego M. Severe complications in testicular germ cell tumors: the choriocarcinoma syndrome. Front Endocrinol (Lausanne) 2019; 10: 218
  • 96 Tian Q, Xue Y, Zheng W. et al. Overexpression of hypoxia-inducible factor 1α induces migration and invasion through Notch signaling. Int J Oncol 2015; 47 (02) 728-738
  • 97 Maruoka Y, Abe K, Baba S. et al. A case of pulmonary choriocarcinoma metastasis with unusual FDG-PET and CT findings: correlation with pathology. Ann Nucl Med 2012; 26 (10) 835-839
  • 98 Gu Q, Yan S, Lin J. et al. Choriocarcinoma masquerading as lung abscess or lung cancer: a case with atypical imaging findings. OncoTargets Ther 2021; 14: 4407-4414
  • 99 Gasparri R, Sedda G, Brambilla D, Girelli L, Diotti C, Spaggiari L. When a differential diagnosis is fundamental: choriocarcinoma mimicking lung carcinoma. J Clin Med 2019; 8 (11) 2018
  • 100 Martínez-Jiménez S, Rosado-de-Christenson ML, Walker CM. et al. Imaging features of thoracic metastases from gynecologic neoplasms. Radiographics 2014; 34 (06) 1742-1754
  • 101 Wegman SJ, Parwani AV, Zynger DL. Cytokeratin 7, inhibin, and p63 in testicular germ cell tumor: superior markers of choriocarcinoma compared to β-human chorionic gonadotropin. Hum Pathol 2019; 84: 254-261
  • 102 Hui P. Gestational choriocarcinoma: a timely review of diagnostic pathology. Arch Pathol Lab Med 2025;
  • 103 Sierra-Bergua B, Sánchez-Marteles M, Cabrerizo-García JL, Sanjoaquin-Conde I. Choriocarcinoma with pulmonary and cerebral metastases. Singapore Med J 2008; 49 (10) e286-e288
  • 104 Li J, Yang J, Liu P. et al. Clinical characteristics and prognosis of 272 postterm choriocarcinoma patients at Peking Union Medical College Hospital: a retrospective cohort study. BMC Cancer 2016; 16 (01) 347
  • 105 Taran F-A, Wosnik A, Juhasz-Böss I, Burtscher K, Morakis P. Clinical routine care for choriocarcinoma: a descriptive analysis of data from the Baden-Wuerttemberg Cancer Registry (BWCR). Arch Gynecol Obstet 2025; 312 (02) 547-554
  • 106 Zhang J, Wang ZJ, Yang B. et al. Biochemical remission by chemoradiotherapy in male mediastinal choriocarcinoma with diffuse lung metastasis: a case report. Oncol Lett 2016; 11 (04) 2615-2618
  • 107 Trapnell BC, Nakata K, Bonella F. et al. Pulmonary alveolar proteinosis. Nat Rev Dis Primers 2019; 5 (01) 16
  • 108 Lettieri S, Bonella F, Marando VA, Franciosi AN, Corsico AG, Campo I. Pathogenesis-driven treatment of primary pulmonary alveolar proteinosis. Eur Respir Rev 2024; 33 (173) 240064
  • 109 Morton C, DeBiasi E. Pulmonary alveolar proteinosis. Clin Chest Med 2025; 46 (02) 373-382
  • 110 Zhang D, Tian X, Feng R. et al. Secondary pulmonary alveolar proteinosis: a single-center retrospective study (a case series and literature review). BMC Pulm Med 2018; 18 (01) 15
  • 111 Liu Y, Chen LL, Qiu YY, Xiao YL, Cai HR. Clinical features of secondary pulmonary alveolar proteinosis associated with myelodysplastic syndrome: two case reports. Medicine (Baltimore) 2017; 96 (44) e8481
  • 112 Ladeb S, Fleury-Feith J, Escudier E, Tran Van Nhieu J, Bernaudin J-F, Cordonnier C. Secondary alveolar proteinosis in cancer patients. Support Care Cancer 1996; 4 (06) 420-426
  • 113 Ishii H, Seymour JF, Tazawa R. et al. Secondary pulmonary alveolar proteinosis complicating myelodysplastic syndrome results in worsening of prognosis: a retrospective cohort study in Japan. BMC Pulm Med 2014; 14 (01) 37
  • 114 Aydin M, Flenaugh EL, Nichols M. Hemoptysis, anemia and respiratory failure: a rare initial presentation of acute leukemia. J Natl Med Assoc 2005; 97 (11) 1550-1552
  • 115 Choi MH, Jung JI, Chung WD. et al. Acute pulmonary complications in patients with hematologic malignancies. Radiographics 2014; 34 (06) 1755-1768
  • 116 Luesink M, Jansen JH. Advances in understanding the pulmonary infiltration in acute promyelocytic leukaemia. Br J Haematol 2010; 151 (03) 209-220
  • 117 Würthner JU, Köhler G, Behringer D, Lindemann A, Mertelsmann R, Lübbert M. Leukostasis followed by hemorrhage complicating the initiation of chemotherapy in patients with acute myeloid leukemia and hyperleukocytosis: a clinicopathologic report of four cases. Cancer 1999; 85 (02) 368-374
  • 118 Azoulay E, Maertens J, Lemiale V. How I manage acute respiratory failure in patients with hematological malignancies. Blood 2024; 143 (11) 971-982
  • 119 Nanjappa S, Jeong DK, Muddaraju M, Jeong K, Hill ED, Greene JN. Diffuse alveolar hemorrhage in acute myeloid leukemia. Cancer Control 2016; 23 (03) 272-277
  • 120 Butler M, Defayette A, Pleskow J, Loecher A, Ross M, Quinn T. Treatment patterns and outcomes of diffuse alveolar hemorrhage: findings from a single-center retrospective study. J Clin Oncol 2023; 41 (16) e19063-e19063
  • 121 Jin SM, Yim JJ, Yoo CG. et al. Aetiologies and outcomes of diffuse alveolar haemorrhage presenting as acute respiratory failure of uncertain cause. Respirology 2009; 14 (02) 290-294
  • 122 Kumasaka S, Kumasaka Y, Jingu A, Tsushima Y. Diagnostic value of “hyperdense consolidation sign” as a characteristic new computed tomography sign of diffuse alveolar hemorrhage. Sci Rep 2022; 12 (01) 21143
  • 123 Ahn JH, Song KM, Huh JW. et al. Corticosteroid therapy for diffuse alveolar hemorrhage with respiratory failure in hematologic malignancies: a retrospective cohort study. Ther Clin Risk Manag 2025; 21: 705-714
  • 124 Schneider BJ, Naidoo J, Santomasso BD. et al. Management of immune-related adverse events in patients treated with immune checkpoint inhibitor therapy: ASCO guideline update. J Clin Oncol 2021; 39 (36) 4073-4126
  • 125 Guo X, Chen S, Wang X, Liu X. Immune-related pulmonary toxicities of checkpoint inhibitors in non-small cell lung cancer: diagnosis, mechanism, and treatment strategies. Front Immunol 2023; 14: 1138483
  • 126 Lin M-X, Zang D, Liu C-G, Han X, Chen J. Immune checkpoint inhibitor-related pneumonitis: research advances in prediction and management. Front Immunol 2024; 15: 1266850
  • 127 Naidoo J, Wang X, Woo KM. et al. Pneumonitis in patients treated with anti-programmed death-1/programmed death ligand 1 therapy. J Clin Oncol 2017; 35 (07) 709-717
  • 128 Cui P, Li J, Tao H. et al. Deciphering pathogenic cellular module at single-cell resolution in checkpoint inhibitor-related pneumonitis. Oncogene 2023; 42 (42) 3098-3112
  • 129 Johkoh T, Lee KS, Nishino M. et al. Chest CT diagnosis and clinical management of drug-related pneumonitis in patients receiving molecular targeting agents and immune checkpoint inhibitors: a position paper from the Fleischner Society. Chest 2021; 159 (03) 1107-1125
  • 130 Carbone RG, Puppo F, Mattar E, Roden AC, Hirani N. Acute and chronic eosinophilic pneumonia: an overview. Front Med (Lausanne) 2024; 11: 1355247
  • 131 Zimmermann N, Wikenheiser-Brokamp KA. Hypereosinophilic syndrome in the differential diagnosis of pulmonary infiltrates with eosinophilia. Ann Allergy Asthma Immunol 2018; 121 (02) 179-185
  • 132 Zanelli M, Smith M, Zizzo M. et al. A tricky and rare cause of pulmonary eosinophilia: myeloid/lymphoid neoplasm with eosinophilia and rearrangement of PDGFRA. BMC Pulm Med 2019; 19 (01) 216
  • 133 Morales-Camacho RM, Caballero-Velázquez T, Borrero JJ, Bernal R, Prats-Martín C. Hematological neoplasms with eosinophilia. Cancers (Basel) 2024; 16 (02) 337
  • 134 Shomali W, Gotlib J. World Health Organization and International Consensus Classification of eosinophilic disorders: 2024 update on diagnosis, risk stratification, and management. Am J Hematol 2024; 99 (05) 946-968
  • 135 Kelemen K, Saft L, Craig FE. et al. Eosinophilia/hypereosinophilia in the setting of reactive and idiopathic causes, well-defined myeloid or lymphoid leukemias, or germline disorders. Am J Clin Pathol 2021; 155 (02) 179-210
  • 136 Cottin V. Eosinophilic lung diseases. Immunol Allergy Clin North Am 2023; 43 (02) 289-322
  • 137 Katre RS, Sunnapwar A, Restrepo CS. et al. Cardiopulmonary and gastrointestinal manifestations of eosinophil- associated diseases and idiopathic hypereosinophilic syndromes: multimodality imaging approach. Radiographics 2016; 36 (02) 433-451