Intrapulmonary unicentric Castleman’s Disease: A clinical analysis of 8 patients

Intrapulmonary unicentric Castleman’s Disease: A clinical analysis of 8 patients

Authors

  • Linling Jin Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
  • Yiting He Department of Respiratory and Critical Care Medicine, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu, China
  • Chenyang Liu Department of Respiratory and Critical Care Medicine, Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu, China
  • Songtao Liu Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
  • Shuying Ma Department of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
  • Nan Li Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
  • Hui Kong Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
  • Weiping Xie Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
  • Mengyu He Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China https://orcid.org/0000-0002-2830-8416

Keywords:

Unicentric Castleman's disease, Intrapulmonary lesion, Clinical features, Surgical resection

Abstract

Background and aims: Castleman’s disease (CD) is a rare, chronic, lymphoproliferative disorder, increasingly recognized as a clonal neoplasm of lymph node stromal cells that can affect multiple organs and tissues. Intrapulmonary unicentric Castleman’s disease (UCD) represents an exceptionally uncommon subtype, primarily involving the lung parenchyma and hilum, with only a few pathologically confirmed cases reported to date. This study aimed to characterize the clinical, radiological, and pathological features of intrapulmonary UCD and to summarize diagnostic and therapeutic experiences.

Methods: We retrospectively analyzed eight patients diagnosed with intrapulmonary UCD. Clinical manifestations, laboratory data, radiologic and bronchoscopic findings, histopathological characteristics, treatment approaches, and follow-up outcomes were systematically reviewed.

Results: No patient exhibited specific clinical symptoms or distinctive laboratory abnormalities. Chest computed tomography (CT) served as the optimal imaging modality, consistently revealing solitary, well-circumscribed, soft-tissue masses with smooth lobulated contours. Definitive diagnosis relied on histopathological examination. All patients underwent complete surgical resection, followed by regular postoperative surveillance with chest CT. During follow-up, no local recurrence or disease progression was detected.

Conclusions: Intrapulmonary UCD is an exceedingly rare form of Castleman’s disease that can be easily misdiagnosed as primary lung tumors, lymphoma, granulomatous disease, or tuberculosis due to its nonspecific clinical and radiological features. Complete surgical excision remains the mainstay of treatment and is associated with an excellent prognosis following complete resection.

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Published

27-03-2026

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Section

Original Articles: Clinical Research

How to Cite

1.
Jin L, He Y, Liu C, Liu S, Ma S, Li N, et al. Intrapulmonary unicentric Castleman’s Disease: A clinical analysis of 8 patients. Sarcoidosis Vasc Diffuse Lung Dis [Internet]. 2026 Mar. 27 [cited 2026 Apr. 17];43(1):18073. Available from: https://mail.mattioli1885journals.com/index.php/sarcoidosis/article/view/18073