[Castleman's disease : a rare differential diagnosis for Heerfordt's syndrome].

作者: R. Hirt , U. Krause , S. Knipping

DOI: 10.1007/S00106-012-2522-1

关键词:

摘要: A 50-year-old male patient demonstrated an existing left proptosis for several weeks. The was suffering from physical exhaustion and had lost considerable weight. Furthermore, we observed greatly enlarged parotid submandibular glands on both sides. MRI of the neck showed multiple, sharply circumscribed lesions in major salivary lacrimal as well orbit. Initially suspected Heerfordt's syndrome, a manifestation sarcoidosis, but laboratory diagnosis could not reveal pathological erythrocyte sedimentation rate or increased ACE titer. After exploratory excision right gland, histological examination revealed Castleman's disease. Therefore, initiated immunomodulatory therapy with interleukin-6 receptor antagonists.Castleman's disease is one very rare, benign, lymphoproliferative processes that have tendency to turn malignant. Isolated findings should be completely resected. There are no clear treatment strategies multiple localizations approaches range systemic glucocorticoid chemotherapy treatment. In contrast isolated findings, prognosis multicentric occurrence unfavorable.

参考文章(11)
Arthur R. Gaba, Richard S. Stein, Donald L. Sweet, Daina Variakojis, Multicentric giant lymph node hyperplasia. American Journal of Clinical Pathology. ,vol. 69, pp. 86- 90 ,(1978) , 10.1093/AJCP/69.1.86
F. H�lzle, A. Landers, C. Platz-Baudin, D. Basrei, K.-D. Wolff, [Castleman's disease]. Mund-, Kiefer- und Gesichtschirurgie : MKG. ,vol. 9, pp. 121- 125 ,(2005) , 10.1007/S10006-004-0592-2
Ettore Bartoli, Giovannino Massarelli, Giovanni Soggia, Francesco Tanda, Multicentric giant lymph node hyperplasia. A hyperimmune syndrome with a rapidly progressive course. American Journal of Clinical Pathology. ,vol. 73, pp. 423- 426 ,(1980) , 10.1093/AJCP/73.3.423
C. Walter, A. Schwarting, T. Hansen, G. Weibrich, Das Heerfordt-Syndrom — eine seltene Erstmanifestation der Sarkoidose Mund-, Kiefer- Und Gesichtschirurgie. ,vol. 9, pp. 43- 47 ,(2005) , 10.1007/S10006-004-0582-4
D. P. Kooper, R. M. Tiwari, P. van der Valk, Castleman's disease as a uncommon cause of a neck mass. European Archives of Oto-rhino-laryngology. ,vol. 251, pp. 370- 372 ,(1994) , 10.1007/BF00171548
Gregory M. Chronowski, Chul S. Ha, Richard B. Wilder, Fernando Cabanillas, John Manning, James D. Cox, Treatment of unicentric and multicentric Castleman disease and the role of radiotherapy. Cancer. ,vol. 92, pp. 670- 676 ,(2001) , 10.1002/1097-0142(20010801)92:3<670::AID-CNCR1369>3.0.CO;2-Q
Benjamin Castleman, Lalla Iverson, V. Pardo Menendez, Localized mediastinal lymph-node hyperplasia resembling thymoma Cancer. ,vol. 9, pp. 822- 830 ,(1956) , 10.1002/1097-0142(195607/08)9:4<822::AID-CNCR2820090430>3.0.CO;2-4
A. Rübberdt, M. Memming, J. Brennecke, J. Jähne, Der Castleman-Tumor als seltene Differentialdiagnose einer cervicalen Raumforderung Chirurg. ,vol. 72, pp. 965- 968 ,(2001) , 10.1007/S001040170097
M. Delos, M. Remacle, J. Ninane, D. Tuerlinckx, E. Bodart, Unifocal cervical Castleman disease in two children. European Journal of Pediatrics. ,vol. 156, pp. 701- 703 ,(1997) , 10.1007/S004310050693
Mohammad Vasef, William E. Katzin, Geoffrey Mendelsohn, Melvin Reydman, Report of a case of localized Castleman's disease with progression to malignant lymphoma. American Journal of Clinical Pathology. ,vol. 98, pp. 633- 636 ,(1992) , 10.1093/AJCP/98.6.633