BMC Pulmonary Medicine | |
Clinical spectrum of intrathoracic Castleman disease: a retrospective analysis of 48 cases in a single Chinese hospital | |
Yi Xiao3  Zuo jun Xu3  Ying zhi Qin4  Cheng Huang4  Rui e Feng1  Ya lan Bi1  Kai Xu2  Jian Cao2  Hui Huang3  Shan Li3  Jin mei Luo3  | |
[1] Pathological Department, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, #1 Shuaifuyuan Street, Dongcheng District 100730, Beijing, China;Radiological Department, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, #1 Shuaifuyuan Street, Dongcheng District 100730, Beijing, China;Department of Respiratory Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, #1 Shuaifuyuan Street, Dongcheng District 100730, Beijing, China;Department of Thoracic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, #1 Shuaifuyuan Street, Dongcheng District 100730, Beijing, China | |
关键词: Clinical characters; Multicentric; Unicentric; Intrathoracic; Castleman disease; | |
Others : 1177627 DOI : 10.1186/s12890-015-0019-x |
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received in 2014-10-17, accepted in 2015-03-06, 发布年份 2015 | |
【 摘 要 】
Background
Thorax is the common place to develop Castleman disease (CD), but there is no systemic clinical analysis for intrathoracic CD.
Methods
We conducted a retrospective analysis of 48 intrathoracic CD patients with definite pathological diagnosis who were hospitalized between 1992 and 2012 in a Chinese tertiary referral hospital.
Results
The study included 16 cases with unicentric CD (UCD) and 32 cases with multicentric CD (MCD). UCD were younger than MCD (30.5y vs 41.6ys, P < 0.05). MCD were more symptomatic (50% vs 96.9%, P < 0.001) and sicker than UCD, including more fever, hepatomegaly and/or splenomegaly and hypoalbuminemia. All of UCD showed solitary mass in various sites and two of them were complicated by small pleural effusion. In the MCD group, their chest CT showed obvious lymphadenopathy in the hilum and/or mediastinum (100%), diffuse parenchymal lung shadows (43.75%), pleural effusion (40.6%), mass in the mediastinum (6.25%) or hilum (3.12%) and bronchiolitis obliterans (BO) (3.12%). Besides LIP-like images, multiple nodules of different size and sites, patchy, ground-glass opacities and consolidation were showed in their chest CT. Surgery were arranged for all UCD for diagnosis and treatment and all were alive. In MCD group, superficial lymph nodes biopsies (21 cases), surgery biopsy (9 cases) and CT-guided percutaneous lung biopsy (2 cases) were performed. Hyaline vascular (HV) variant were more common in the UCD group (75% vs 37.5%, P < 0.05). In MCD group, 28 cases were prescribed with chemotherapy, one refused to receive therapy and the rest three were arranged for regular follow-up. Among MCD, 18 cases was improved, 7 cases was stable, 4 cases lost follow-up and 3 cases died.
Conclusions
Intrathoracic MCD was more common than UCD in our hospital. MCD was older, more symptomic and sicker than UCD. HV variant were more common in UCD. All of UCD showed mass in various intrathoracic locations and surgery resection was performed for all and all were alive. Mass, pleural effusion, BO and diffuse pulmonary shadows, including LIP-like images, multiple nodules of different size and sites, patchy, GGO and consolidations were showed in our MCD. Most of MCD cases were arranged with chemotherapy and their prognosis were worse than UCD’s.
【 授权许可】
2015 Luo et al.; licensee BioMed Central Ltd.
【 预 览 】
Files | Size | Format | View |
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20150503020453947.pdf | 2146KB | download | |
Figure 2. | 100KB | Image | download |
Figure 1. | 95KB | Image | download |
【 图 表 】
Figure 1.
Figure 2.
【 参考文献 】
- [1]Dispenzieri A, Armitage JO, Loe MJ, Geyer SM, Allred J, Camoriano JK, Menke DM, Weisenburger DD, Ristow K, Dogan A, Habermann TM: The clinical spectrum of Castleman’s disease. Am J Hematol 2012, 87:997-1002.
- [2]Talat N, Schulte KM: Castleman’s disease: systematic analysis of 416 patients from the literature. Oncologist 2011, 16:1316-1324.
- [3]Zhu SH, Yu YH, Zhang Y, Sun JJ, Han DL, Li J: Clinical features and outcome of patients with HIV-negative multicentric Castleman’s disease treated with combination chemotherapy: a report on 10 patients. Med Oncol 2013, 30:492.
- [4]Kim JH, Jun TG, Sung SW, Shim YS, Han SK, Kim YW, Yoo CG, Seo JW, Rho JR: Giant lymph node hyperplasia (Castleman’s disease) in the chest. Ann Thorac Surg 1995, 59:1162-1165.
- [5]Ko SF, Wan YL, Ng SH, Lin JW, Hsieh MJ, Fang FM, Lee TY, Chen WJ: Imaging features of atypical thoracic Castleman disease. Clin Imaging 2004, 28:280-285.
- [6]Kwon S, Lee KS, Ahn S, Song I, Kim TS: Thoracic Castleman disease: computed tomography and clinical findings. J Comput Assist Tomogr 2013, 37:1-8.
- [7]Burrah R, Deshmane V, Althaf S, Yapamakula S, Kurubabala S, Hanumaiah A, Kumar V: Castleman’s disease of the pleura. Gen Thorac Cardiovasc Surg 2011, 59:572-574.
- [8]Yu JY, Oh IJ, Kim KS, Kim YI, Lim SC, Kim YC, Choi YD, Kwon YS: Castleman’s disease presenting as a tracheal mass. Ann Thorac Surg 2014, 97:1798-1800.
- [9]Nikolskaia OV, Nousari CH, Anhalt GJ: Paraneoplastic pemphigus in association with Castleman’s disease. Br J Dermatol 2003, 149:1143-1151.
- [10]Chin AC, Stich D, White FV, Radhakrishnan J, Holterman MJ: Paraneoplastic pemphigus and bronchiolitis obliterans associated with a mediastinal mass: a rare case of Castleman’s disease with respiratory failure requiring lung transplantation. J Pediatr Surg 2001, 36:E22.
- [11]Awotedu AA, Otulana BA, Ukoli CO: Giant lymph node hyperplasia of the lung (Castleman’s disease) associated with recurrent pleural effusion. Thorax 1990, 45:775-776.
- [12]Ko SF, Ng SH, Hsieh MJ, Lin JW, Huang CC, Lee TY, Chen WJ: Castleman disease of the pleura: experience with eight surgically proven cases. Ann Thorac Surg 2003, 76:219-224.
- [13]Gunluoglu G, Olcmen A, Sokucu SN, Akin H, Dincer I: Intrapulmonary-located Castleman’s disease, which was surgically resected without pulmonary resection. Ann Thorac Cardiovasc Surg 2011, 17:580-583.
- [14]Hwangbo Y, Cha SI, Lee YH, Lee SY, Seo H, Oh S, Kim M, Choi SH, Park TI, Shin KM: A case of multicentric Castleman’s disease presenting with follicular bronchiolitis. Tuberc Respir Dis (Seoul) 2013, 74:23-27.
- [15]Johkoh T, Muller NL, Ichikado K, Nishimoto N, Yoshizaki K, Honda O, Tomiyama N, Naitoh H, Nakamura H, Yamamoto S: Intrathoracic multicentric Castleman disease: CT findings in 12 patients. Radiology 1998, 209:477-481.
- [16]Iyonaga K, Ichikado K, Muranaka H, Fujii K, Yamaguchi T, Suga M: Multicentric Castleman’s disease manifesting in the lung: clinical, radiographic, and pathologic findings and successful treatment with corticosteroid and cyclophosphamide. Intern Med 2003, 42:182-186.
- [17]Keller AR, Hochholzer L, Castleman B: Hyaline-vascular and plasma-cell types of giant lymph node hyperplasia of the mediastinum and other locations. Cancer 1972, 29:670-683.
- [18]Cronin DM, Warnke RA: Castleman disease: an update on classification and the spectrum of associated lesions. Adv Anat Pathol 2009, 16:236-246.
- [19]Shin DY, Jeon YK, Hong YS, Kim TM, Lee SH, Kim DW, Kim I, Yoon SS, Heo DS, Park S, Kim BK: Clinical dissection of multicentric Castleman disease. Leuk Lymphoma 2011, 52:1517-1522.
- [20]Ye B, Gao SG, Li W, Yang LH, Zhao SH, Ma K, Zhu XL, Liu XY, Sun KL: A retrospective study of unicentric and multicentric Castleman’s disease: a report of 52 patients. Med Oncol 2010, 27:1171-1178.
- [21]Milanovic N, Matkovic S, Ristic D, Jelic S, Petrovic M: Significance of tumor burden, vascular endothelial growth factor, lactate dehydrogenase and beta-2 microglobulin serum levels in advanced diffuse large B cell lymphoma. J BUON 2012, 17:497-501.
- [22]De Marchi G1, De Vita S, Fabris M, Scott CA, Ferraccioli G: Systemic connective tissue disease complicated by Castleman’s disease: report of a case and review of the literature. Haematologica 2004, 89:ECR03.
- [23]Guihot A, Couderc LJ, Agbalika F, Galicier L, Bossi P, Rivaud E, Scherrer A, Zucman D, Katlama C, Oksenhendler E: Pulmonary manifestations of multicentric Castleman’s disease in HIV infection: a clinical, biological and radiological study. Eur Respir J 2005, 26:118-125.
- [24]Guihot A, Couderc LJ, Rivaud E, Galicier L, Bossi P, Oksenhendler E, Scherrer A: Thoracic radiographic and CT findings of multicentric Castleman disease in HIV-infected patients. J Thorac Imaging 2007, 22:207-211.
- [25]McAdams HP, Rosado-de-Christenson M, Fishback NF, Templeton PA: Castleman disease of the thorax: radiologic features with clinical and histopathologic correlation. Radiology 1998, 209:221-228.
- [26]Sheng L, Cao WK: HIV/AIDS epidemiology and prevention in China. Chin Med J (Engl) 2008, 121:1230-1236.
- [27]Robinson D Jr, Reynolds M, Casper C, Dispenzieri A, Vermeulen J, Payne K, Schramm J, Ristow K, Desrosiers MP, Yeomans K, Teltsch D, Swain R, Habermann TM, Rotella P, Van de Velde H: Clinical epidemiology and treatment patterns of patients with multicentric Castleman disease: results from two US treatment centres. Br J Haematol 2014, 165:39-48.
- [28]Waterston A, Bower M: Fifty years of multicentric Castleman’s disease. Acta Oncol 2004, 43:698-704.
- [29]Kawabata H, Kadowaki N, Nishikori M, Kitawaki T, Kondo T, Ishikawa T, Yoshifuji H, Yamakawa N, Imura Y, Mimori T, Matsumura Y, Miyachi Y, Matsubara T, Yanagita M, Haga H, Takaori-Kondo A: Clinical features and treatment of multicentric castleman’s disease: a retrospective study of 21 Japanese patients at a single institute. J Clin Exp Hematop 2013, 53:69-77.
- [30]Casper C: The aetiology and management of Castleman disease at 50 years: translating pathophysiology to patient care. Br J Haematol 2005, 129:3-17.
- [31]Dossier A, Meignin V, Fieschi C, Boutboul D, Oksenhendler E, Galicier L: Human herpesvirus 8-related Castleman disease in the absence of HIV infection. Clin Infect Dis 2013, 56:833-842.
- [32]Kurai M, Kondo R, Kobayashi N, Hyogotani A, Yoshida K, Amano J: Castleman’s disease arising from the chest wall. Jpn J Thorac Cardiovasc Surg 2006, 54:555-557.
- [33]Ueda H, Kouso H, Tsukamoto S: Castleman’s disease of the chest wall. J Thorac Oncol 2009, 4:426-428.
- [34]Pham TT, Harrell JH, Harrell JH, Herndier B, Yi ES: Endotracheal castleman disease: a case report. Chest 2007, 131:590-592.
- [35]Pinheiro VG, Fernandes GH, Cezar LC, Alves NA, de Menezes DB: Castleman’s disease accompanied by pleural effusion. J Bras Pneumol 2008, 34:626-630.
- [36]Jindal T, Meena M, Kumar A, Khaitan BK: Paraneoplastic pemphigus with Castleman’s disease and bronchiolitis obliterans. Pediatr Int 2011, 53:1108-1109.
- [37]Pejaver RK, Watson AH: Castleman’s disease. Respir Med. 1994, 88:309-311.
- [38]Gupta NK, Torigian DA, Gefter WB, Marshall MB, Liang H, Carver JR, Miller WT Jr: Mediastinal Castleman disease mimicking mediastinal pulmonary sequestration. J Thorac Imaging 2005, 20:229-232.
- [39]Slater BJ, Nordin AB, Allen CE, Elghetany MT, Heinle JS, Kim ES: Resection of mediastinal castleman’s disease: a case report. Pediatr Hematol Oncol 2013, 30:554-6.
- [40]Stavridis GT, Lau OJ: Castleman’s disease arising from the intercostal space. Eur J Cardiothorac Surg 1993, 7:218-219.
- [41]Yeh CM, Chou CM, Wong LC: Castleman’s disease mimicking intrapulmonary malignancy. Ann Thorac Surg 2007, 84:e6-7.
- [42]Blankenship ME, Rowlett J, Timby JW, Roth RS, Jones RE: Giant lymph node hyperplasia (Castleman’s disease) presenting with chylous pleural effusion. Chest 1997, 112:1132-1133.
- [43]Light RW: The Light criteria: the beginning and why they are useful 40 years later. Clin Chest Med 2013, 34:21-26.