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Solitary infantile and adult myofibromatosis of the nasal cavity: a report of two cases

Published online by Cambridge University Press:  29 June 2007

R. M. Walsh*
Affiliation:
Department of OtolaryngologyGuys HospitalSt Thomas Street, London SE1 9RT, UK.
E. J. Leen
Affiliation:
Departments of Histopathology, Guys Hospital, St Thomas Street, London SE1 9RT, UK.
M. J. Gleeson
Affiliation:
Department of OtolaryngologyGuys HospitalSt Thomas Street, London SE1 9RT, UK.
*
Address for correspondence: Mr Rory M. Walsh, F.R.C.S., Department of Otolaryngology, North Staffordshire Royal Infirmary, Stoke on Trent, Staffordshire ST4 7LN.

Abstract

Myofibromatosis is an uncommon, usually cutaneous, condition in which there is a benign proliferation of myofibroblasts. Solitary and multicentric nodular forms with, and without, visceral involvement have been described. Infantile and adult sub-types have been reported, each having distinct clinicopathological features. Presentation in the head and neck is common. It is frequently misdiagnosed because of its peculiar histological features. The first documented cases of infantile and adult myofibromatosis involving the nasal cavity are reported.

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 1996

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References

Beham, A., Badve, S., Suster, S., Fletcher, C. D. M. (1993) Solitary myofibroma in adults: clinicopathological analysis of a series. Histopathology 22: 335341.CrossRefGoogle ScholarPubMed
Benjamin, S. P., Mercer, R. D., Hawk, W. A. (1977) Myofibroblastic contraction in spontaneous regression of multiple congenital mesenchymal hamartomas. Cancer 40: 23432352.3.0.CO;2-L>CrossRefGoogle ScholarPubMed
Briselli, M. F., Soule, E. H., Gilchrist, G. S. (1980) Congenital fibromatosis: report of 18 cases of solitary and four cases of multiple tumours. Mayo Clinic Proceedings 55: 554562.Google Scholar
Chung, E. B., Enzinger, F. M. (1981) Infantile myofibromatosis. Cancer 48: 18071818.3.0.CO;2-G>CrossRefGoogle ScholarPubMed
Daimaru, Y., Hashimoto, H., Enjoji, M. (1989) Myofibromatosis in adults (adult counterpart of infantile myofibromatosis). American Journal of Surgical Pathology 13: 859865.CrossRefGoogle ScholarPubMed
Fletcher, C. D. M., Achu, P., Van Noorden, S., McKee, P. H. (1987) Infantile myofibromatosis: a light microscopic, histochemical and immunohistochemical study suggesting true smooth muscle differentiation. Histopathology 11: 245258.CrossRefGoogle ScholarPubMed
Hartig, G., Koopmann, G., Esclamado, R. (1993) Infantile myofibromatosis: a commonly misdiagnosed entity. Otolaryngology – Head and Neck Surgery 109: 753757.CrossRefGoogle ScholarPubMed
Hogan, S. F., Salassa, J. R. (1992) Recurrent adult myofibromatosis. A case report. American Journal of Clinical Practice 97: 810814.Google ScholarPubMed
Jennings, T. A., Duray, P. H., Collins, F. S., Sabettlon, J., Enzinger, F. M. (1984) Infantile myofibromatosis. Evidence for an autosomal dominant disorder. American Journal of Surgical Pathology 7: 529538.CrossRefGoogle Scholar
Kauffmann, S. L., Stout, A. P. (1965) Congenital mesenchymal tumours. Cancer 18: 460476.3.0.CO;2-B>CrossRefGoogle Scholar
Sleeman, D. J., Eveson, J. W. (1991) Solitary infantile myofibromatosis. British Journal of Oral and Maxillofacial Surgery 29: 277278.CrossRefGoogle ScholarPubMed
Smith, K. J., Skelton, H. G., Barrett, T. L., Lupton, G. P., Graham, J. H. (1989) Cutaneous myofibroma. Modern Pathology 2: 603609.Google ScholarPubMed
Speight, P. M., Dayan, D., Fletcher, C. D. M. (1991) Adult and infantile myoflbromatosis: a report of three cases affecting the oral cavity. Journal of Oral Pathology and Medicine 20: 380384.CrossRefGoogle ScholarPubMed
Stout, A. P. (1954) Juvemle fibromatosis. Cancer 7: 953978.3.0.CO;2-W>CrossRefGoogle Scholar
Vigneswaran, N., Boyd, D. L., Waldron, C. A. (1992) Solitary infantile myofibromatosis of the mandible. Report of three cases. Oral Surgery, Oral Medicine, Oral Pathology 73: 84:88.CrossRefGoogle ScholarPubMed