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  Vol. 125 No. 1, January 1999 TABLE OF CONTENTS
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Pediatric Myofibromatosis of the Head and Neck

Jill C. Beck, MD; Kenneth O. Devaney, MD; Robert A. Weatherly, MD; Charles F. Koopmann, Jr, MD; Marci M. Lesperance, MD

Arch Otolaryngol Head Neck Surg. 1999;125:39-44.

Objectives  To examine the clinical and pathological features of pediatric myofibroma of the head and neck and to discuss the challenges in diagnosis and treatment.

Design  A retrospective search of pathology department and clinical records to identify patients with myofibroma and a retrospective review of English-language medical publications.

Setting  Academic medical center.

Patients  Thirteen pediatric patients (aged from birth to 8 years old) diagnosed as having myofibroma of the head and neck.

Results  Nine of 13 patients were cured with conservative surgical excision. Four patients (31%) had recurrence, requiring multiple surgical procedures. One third showed spontaneous regression clinically or by histological examination. The clinical course did not parallel the histological appearance, as high cellularity and mitotic figures were commonplace among the specimens. A misdiagnosis of malignancy was not unusual in this series, as 3 patients had an initial diagnosis of fibrosarcoma, which on review was revised to myofibroma.

Conclusions  Myofibromatosis is a distinct disorder among the great number of fibrous proliferations occurring in infants and children, with a particular predilection for the head and neck region. These lesions should be clearly distinguished from conventional adult-type fibromatoses (desmoid tumors), which are more aggressive. Most patients have solitary lesions that respond well to conservative surgical excision, whereas a few of these lesions behave more aggressively, requiring several surgical procedures for the management of recurrent or persistent tumor. Many of these lesions show spontaneous regression, suggesting that lesions not affecting vital functions, resulting in growth anomalies, or demonstrating rapid aggressive growth may be managed conservatively.


From the Division of Pediatric Otolaryngology (Drs Weatherly, Koopmann, and Lesperance), Department of Otolaryngology–Head and Neck Surgery (Drs Beck, Weatherly, Koopmann, and Lesperance), and Department of Pathology (Dr Devaney), University of Michigan Health System, Ann Arbor.



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