Elsevier

Auris Nasus Larynx

Volume 33, Issue 1, March 2006, Pages 93-96
Auris Nasus Larynx

Myxofibrosarcoma of the hypopharynx

https://doi.org/10.1016/j.anl.2005.07.004Get rights and content

Abstract

Myxofibrosarcoma is common in the extremities, but rare in the head and neck region. Hypopharyngeal myxofibrosarcoma has not been reported previously. We report the first case of a patient with myxofibrosarcoma of the hypopharynx. We examined this patient once a month after the operation, and there has been no local recurrence and no distant metastasis. Sarcomas are rare in the hypopharynx, but we have to bear in mind their possibility. Though a low-grade myxofibrosarcoma is a low-grade malignancy, complete resection should be done. We have to pay more attention planning the treatment for neoplastic diseases.

Introduction

Myxofibrosarcoma is one of the commonest sarcomas in the field of orthopedic surgery. Typically, it grows in the subcutaneous of the extremities of elderly persons. Myxofibrosarcoma in the head and neck region is very rare and only a few cases of the disease in this area have been reported [1], [2], [3]. Most of the malignant tumors in the hypopharynx are carcinomas, and there are some reports of hypopharyngeal sarcomas, such as angiosarcoma, follicular dendritic cell sarcoma, liposarcoma and synovial sarcoma [6], [7], [8], [9]. Here, we report a first case of hypopharyngeal myxofibrosarcoma.

Section snippets

Case report

A 69-year-old Japanese man had a gastrointestinal fiberscope examination, which he had been receiving every year for the health check-up, by an internal medicine doctor at a municipal hospital in June 2003. The doctor found a tumor in the larynx and consulted an otorhinolaryngologist (ORL). The ORL doctor diagnosed it as a hypopharyngeal tumor and introduced this patient to our hospital. He had been suffering from hypertension for more than 10 years with good control and had a history of brain

Discussion

Myxofibrosarcoma was first proposed by Angervall et al. [10], who described it as a group of fibroblastic lesions which has cellular distribution, pleomorphism of the nucleus, and mitotic activity that varies from a less cellular lesion with minimal cytologic atypia to a more cellular lesion with features similar to those of pleomorphic-storiform malignant fibrous histiocytoma (MFH). Histological findings at low magnification show many nodules with low cellularity. The component cells are

Acknowledgements

We thank Dr. N. Kameda, Department of Pathology, Sakura Hospital, Toho University, Dr. H. Hashimoto, Department of Pathology and Oncology, School of Medicine, University of Occupational and Environmental Health, Dr. H. Kanda, Department of Pathology, The Cancer Institute of the Japanese Foundation for Cancer Research and Dr. M. Tsuneyoshi, Department of Anatomic Pathology, Graduate School of Medicine, Kyushu University, for pathological diagnose.

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