Hostname: page-component-78c5997874-mlc7c Total loading time: 0 Render date: 2024-11-19T15:26:19.983Z Has data issue: false hasContentIssue false
  • English
  • Français

Castleman's disease restricted to the infratemporal fossa

Published online by Cambridge University Press:  29 June 2007

Juan P. Rodrigo ,
Jose A. Fernandez ,
Juan C. Alvarez ,
Justo Gómez  and
Carlos Suárez
Juan P. Rodrigo*
Affiliation:
Department of Otolaryngology, Hospital Central de Asturias, University of Oviedo, Oviedo, Spain.
Jose A. Fernandez
Affiliation:
Department of Otolaryngology, Hospital Central de Asturias, University of Oviedo, Oviedo, Spain.
Juan C. Alvarez
Affiliation:
Department of Otolaryngology, Hospital Central de Asturias, University of Oviedo, Oviedo, Spain.
Justo Gómez
Affiliation:
Department of Otolaryngology, Hospital Central de Asturias, University of Oviedo, Oviedo, Spain.
Carlos Suárez
Affiliation:
Department of Otolaryngology, Hospital Central de Asturias, University of Oviedo, Oviedo, Spain.
*
Address for correspondence: Juan P. Rodrigo, C/ Fernández Ladreda 32-A 420B, 33011 Oviedo, Spain. Fax: 34-8-5108015
Get access Rights & Permissions [Opens in a new window]

Abstract

Giant lymph node hyperplasia (Castleman's disease) is usually reported as a solitary mediastinal tumour, although involvement of other anatomical sites and a multicentric form have been reported. We describe a rare case of Castleman's disease due to its localisation (the left infratemporal fossa) and histology (plasma-cell variant). A brief review of the main clinico-histological characteristics of Castleman's disease is also presented.

Keywords

Giant lymph node hyperplasiaHead and neck neoplasms
Type
Clinical Records
Information
The Journal of Laryngology & Otology , Volume 110 , Issue 9 , September 1996 , pp. 896 - 898
Copyright
Copyright © JLO (1984) Limited 1996

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Castleman, B., Towne, V. W. (1954) Case records of the Massachussets General Hospital. New England Journal of Medicine 250: 26–30.Google Scholar
Castleman, B., Iverson, M., Menéndez, V. (1956) Localized mediastinal lymph node hyperplasia resembling thymoma. Cancer 9: 822–830.3.0.CO;2-4>CrossRefGoogle Scholar
Chaloupka, J. C, Castillo, M., Hudgins, P. (1990) Castleman disease in the neck: atypical appearance on CT. American Journal of Roentgenology 154: 1051–1052.CrossRefGoogle ScholarPubMed
Chan, M. K., McGuire, L. J. (1992) Cytodiagnosis of lesions presenting as salivary gland swellings: a report of seven cases. Diagnostic Cytopathology 8: 439–443.CrossRefGoogle ScholarPubMed
Climie, A. R. W., Waggoner, L. G., Krabbenhoft, K. L. (1964) Lymphoid hamartoma of the larynx. Laryngoscope 74: 1381–1383.Google ScholarPubMed
Cohen, H. (1957) Tumour-like proliferations of lymphoid tissue: Occurrence in deltoid muscle and mediastinum. Journal of Mount Sinai Hospital 24: 750–760.Google ScholarPubMed
Daley, M., Gorog, J. L. (1967) Pelvis retroperitoneal lymphoid hamartoma. Journal of Urology 97: 235–242.CrossRefGoogle Scholar
Fisher, E. R., Sierracki, J. C, Goldensberg, M. D. (1970) Identity and nature of isolated tumours (so called nodal hyperplasia, hamartoma and angiomatous hamartoma) as revealed by histologic, electron microscopic and heterotransplantation studies. Cancer 25: 1286–1300.3.0.CO;2-U>CrossRefGoogle ScholarPubMed
Frizzera, G., Peterson, B. A., Bayrd, E. D., Goldman, A. (1985) A systemic lymphoproliferative disorder with morphologic features of Castleman's disease. Clinical findings and clinicopathologic correlations in 15 patients. Journal of Clinical Oncology 3: 1202–1216.CrossRefGoogle ScholarPubMed
Gaba, A. P., Stein, R. S., Sweet, D. L., Variakojis, D. (1978) Multicentric giant lymph node hyperplasia. American Journal of Clinical Pathology 69: 86–90.CrossRefGoogle ScholarPubMed
Gleeson, M. J., Cassidy, M., McMullin, J. P. (1988) Castleman's disease. An unusual neck mass. Journal of Laryngology and Otology 102: 661–663.CrossRefGoogle ScholarPubMed
Keller, A. R., Hochholzer, L., Castleman, B. (1972) Hyaline vascular and plasma cells types of giant lymph node hyperplasia of the mediastinum and other locations. Cancer 29: 670–683.3.0.CO;2-#>CrossRefGoogle ScholarPubMed
Lanier, B. J., Cummings, C. W. (1982) Giant lymph node hyperplasia presenting as a highly vascularized parapharyngeal mass. Otolaryngology-Head and Neck Surgery 90: 426–430.CrossRefGoogle ScholarPubMed
Lattes, R., Pachter, M. R. (1962) Benign lymphoid masses of probable hamartomatous nature. Cancer 15, 197–202.3.0.CO;2-6>CrossRefGoogle ScholarPubMed
Mackay, J. G. (1969) Axillary angiofollicular lymphoid hyperplasia. Canadian Medical Association Journal 100: 434–440.Google Scholar
Penfold, C. N., Cottrell, B. J., Talbot, R. (1991) Neonatal giant lymph node hyperplasia (Castleman's disease) presenting in the head and neck. British Journal of Maxillofacial Surgery 29: 110–111.CrossRefGoogle ScholarPubMed
Pujari, B. D., Deodhares, S. G. (1977) Cervical angiofollicular lymph node hyperplasia (lymphoid hamartoma). Journal of Laryngology and Otology 91: 541–547.CrossRefGoogle ScholarPubMed
Rotenberg, M., Charial, J. P., Cauchois, R., Menard, M., Brasnu, D., Laccourreye, H. (1990) La maladie de Castleman. A propos de deux observations ORL. Annales d'Otolaryngologie et Chirurgie Cervicofaciale 107: 490–493.Google Scholar
Sanz, C., Sierra, J., Cobarro, J., Avellaneda, R., Monserrat, E., Rozman, C. (1992) An unusual case of Castleman's disease restricted to the neck. ORL Journal of Otorhinolaryngology and Related Specialities 54: 331–333.CrossRefGoogle ScholarPubMed
Yi, A. Y., de Tar, M., Becker, T. S., Rice, D. H. (1995) Giant lymph node hyperplasia of the head and neck (Castleman's disease): a report of five cases. Otolaryngology-Head and Neck Surgery 113: 462–466.CrossRefGoogle ScholarPubMed