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Aggressive angiomyxoma of supraclavicular fossa: A case report
Author(s) -
Pai ChienYu,
Nieh Shin,
Lee JihChin,
Lo ChungPing,
Lee HerngSheng
Publication year - 2008
Publication title -
head and neck
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.012
H-Index - 127
eISSN - 1097-0347
pISSN - 1043-3074
DOI - 10.1002/hed.20747
Subject(s) - aggressive angiomyxoma , medicine , head and neck , fossa , histopathology , anatomy , pelvis , radiology , pathology , surgery
Background Aggressive angiomyxoma (AAM) is a rare myxoid mesenchymal tumor that occurs almost exclusively in the adult pelvic‐perineal region and predominantly in females. Only 1 case of AAM occurring outside this region has been reported. Here we report another such case. Methods The patient was referred for evaluation of a firm nonmovable mass of the supraclavicular fossa that had progressively enlarged within the previous year. MRI showed an infiltrative growth pattern with adhesion to adjacent anatomic structures. Wide excision was attempted, but a clear margin could not be achieved. Results The histopathology revealed characteristic features of AAM, including stellate to spindle‐shaped tumor cells set in a myxoid background, with hyalinizing thick‐walled vessels and characteristic immunophenotype. Conclusion Accurate diagnosis and a definite surgical margin are crucial because AAM is locally aggressive and easily recurrent. Our case deserves attention because it shows that AAM may exist in the head and neck. © 2008 Wiley Periodicals, Inc. Head Neck, 2008