Protuberant Fibro-osseous Lesions of the Temporal Bone Two Additional Case Reports

被引:0
作者
Lee, Miji [1 ]
Song, Joon Seon [1 ]
Chun, Sung-Min [1 ,4 ]
Lee, Jeong Hyun [2 ]
Hong, Suk Ho [3 ]
Cho, Kyung-Ja [1 ]
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Pathol, Seoul 138736, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Radiol, Seoul 138736, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurosurg, Seoul 138736, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Asan Ctr Canc Genome Discovery,ASAN Inst Life Sci, Seoul 138736, South Korea
关键词
temporal bone; fibro-osseous lesion; bone tumor; GNAS mutation; MCCUNE-ALBRIGHT-SYNDROME; FIBROUS DYSPLASIA; GS-ALPHA; MUTATIONS; GENE;
D O I
暂无
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The most commonly encountered fibro-osseous lesions of the skull bone are fibrous dysplasia and ossifying fibroma. Two cases of a unique "protuberant fibro-osseous lesion of the temporal bone" were first described by Selesnick and colleagues in 1999, and 2 further cases were reported in 2010 under the name "Bullough lesion". We recently found 2 new cases of this rare entity. Two Korean female patients aged 70 and 54 years presented with slow growing postauricular masses without pain or tenderness for 6 and 7 years, respectively. Computed tomography revealed a 2.9 cm calcified mass in the temporal bone of the first patient, and a 5.5 cm enhancing mass with internal cartilaginous matrix in the temporal bone of the second patient. Intramedullary or intracranial extension was not found in either case, and en bloc removals were performed. Microscopically, multiple round to oval osseous islands were scattered throughout the bland fibrous stroma in both cases. The osseous islands varied in size and were lamellar or woven, without osteoblastic rimming, and surrounded by fibroblastic bands. Neither patient has shown evidence of postoperative recurrence for 18 months. The location, histology, and clinical course of these 2 cases were identical to the 4 cases previously reported, although age and sex varied. The lesions were tested for the R201H mutation in the GNAS gene, which is present in fibrous dysplasia. No mutations were found, suggesting a different genetic background for these lesions.
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页码:1510 / 1515
页数:6
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