A case of fibrous dysplasia occurred centering in the maxilla and its review of the literature
Fibrous dysplasia is a clinical syndrome generally classified into the following three types; Albright's syndrome, polyostotic fibrous dysplasia, and monostotic fibrous dysplasia. However, its classification has diverse pathological meanings, and due to its necessity of differentiating from ost...
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Published in | Japanese Journal of Oral and Maxillofacial Surgery Vol. 36; no. 8; pp. 1874 - 1880 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Japanese Society of Oral and Maxillofacial Surgeons
1990
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Abstract | Fibrous dysplasia is a clinical syndrome generally classified into the following three types; Albright's syndrome, polyostotic fibrous dysplasia, and monostotic fibrous dysplasia. However, its classification has diverse pathological meanings, and due to its necessity of differentiating from osteoid diseases and of selecting an appropriate surgical method a more rational classification is currently required. Thoma proposed that fibrous dysplasia occurring in the maxilla or facial bone should be standardized as facial fibrous dysplasia for discrimineting from the three types mentioned above based on its anatomical peculiarity. Recently, the authors encountered a case of facial fibrous dysplasia as noted by Thoma, the outline of which is reported after discussion of the literatures. The patient, a 17-year-old female, visited our hospital complaining of swelling in the left portion of the exterior bucca. Her case-history revealed that she had noticed the above mentioned symptoms at approximately 13 years of age which were however ignored because of absence of accompanied other subjective symptoms. Recently, she consulted a hospital dentist after the aforementioned swelling had been pointed out by her friends. On the radiogram, diffuse non-permeable images of the maxillary sinus (left side) were observed and the patient was then referred to our department. The swelling was non-symmetry and extended from the zygomatic arch on the left side to the maxillary alveolar region. Radiographic findings showed a non-permeable image with an appearance of frosted glass centering on the maxillary sinus of the left side, which involved all the roots of 3 to 7. A biopsy was performed under a clinical diagnosis of fibrous dysplasia and enucleation was then conducted under general anesthesia. The operation did not proceed with a method exclusively concentrated on the tumor because of its anatomical specificity but initial consideration was given primarily to the reappearance of maxillary sinus morphology and the measurement of the right and left facial symmetry, followed by practicable curettage and enucleation. Pathological and histologic findings revealed that the maxillary sinus was comprised of irregular bone trabecula and fibrous connective tissue, and the former was consisted of in laminar structure and osteoid regions. The postoperative prognosis was favorable, showing no abnormal findings even after a year and four months. |
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AbstractList | Fibrous dysplasia is a clinical syndrome generally classified into the following three types; Albright's syndrome, polyostotic fibrous dysplasia, and monostotic fibrous dysplasia. However, its classification has diverse pathological meanings, and due to its necessity of differentiating from osteoid diseases and of selecting an appropriate surgical method a more rational classification is currently required. Thoma proposed that fibrous dysplasia occurring in the maxilla or facial bone should be standardized as facial fibrous dysplasia for discrimineting from the three types mentioned above based on its anatomical peculiarity. Recently, the authors encountered a case of facial fibrous dysplasia as noted by Thoma, the outline of which is reported after discussion of the literatures. The patient, a 17-year-old female, visited our hospital complaining of swelling in the left portion of the exterior bucca. Her case-history revealed that she had noticed the above mentioned symptoms at approximately 13 years of age which were however ignored because of absence of accompanied other subjective symptoms. Recently, she consulted a hospital dentist after the aforementioned swelling had been pointed out by her friends. On the radiogram, diffuse non-permeable images of the maxillary sinus (left side) were observed and the patient was then referred to our department. The swelling was non-symmetry and extended from the zygomatic arch on the left side to the maxillary alveolar region. Radiographic findings showed a non-permeable image with an appearance of frosted glass centering on the maxillary sinus of the left side, which involved all the roots of 3 to 7. A biopsy was performed under a clinical diagnosis of fibrous dysplasia and enucleation was then conducted under general anesthesia. The operation did not proceed with a method exclusively concentrated on the tumor because of its anatomical specificity but initial consideration was given primarily to the reappearance of maxillary sinus morphology and the measurement of the right and left facial symmetry, followed by practicable curettage and enucleation. Pathological and histologic findings revealed that the maxillary sinus was comprised of irregular bone trabecula and fibrous connective tissue, and the former was consisted of in laminar structure and osteoid regions. The postoperative prognosis was favorable, showing no abnormal findings even after a year and four months. |
Author | MARUTA, Osamu HASEGAWA, Hideyuki SHIRAKAWA, Masayori NOMURA, Takeshi SAKAI, Nobuoki |
Author_xml | – sequence: 1 fullname: HASEGAWA, Hideyuki organization: Department of Dent. Oral and Maxillofacial Surgery, Yokohama Seamen's Insurance Hospital – sequence: 2 fullname: SHIRAKAWA, Masayori organization: Department of Oral and Maxillofacial Surgery, Machida City Hospital – sequence: 3 fullname: MARUTA, Osamu organization: Department of Dent. Oral and Maxillofacial Surgery, Yokohama Seamen's Insurance Hospital – sequence: 4 fullname: NOMURA, Takeshi organization: Department of Oral and Maxillofacial Surgery, Machida City Hospital – sequence: 5 fullname: SAKAI, Nobuoki organization: Department of Oral and Maxillofacial Surgery, Machida City Hospital |
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References | 7) Lichtenstein, L.: Polyostotic fibrous dysplasia. Arch Surg 36: 874-898 1938. 10) 加藤正, 蒲原宏, 他: Fibrous dysplasia of boneの検討. 整形外科19: 630-641 1968. 6) Albright, F., Butler, A. M. et al.: Syndrome characterized by osteitis fibrosa disseminate, areas of pigmentation and endcrine dysfunction, with precocious puberty in females; report of five cases. New Eng J Med 216: 727-746 1937. 9) Montgomery, A. H.: Ossifying fibromas of the jaw. Arch Surg 15: 30-44 1927. 11) McCune, D. J. and Bruch. H.: Osteodystrophia fibrosa; report of a case in which the condition was combined with a precocious puberty, pathologic pigmentation of the skin and hyperthyroidism, with a review of the literature. Amer J Dis Child 54: 806-848 1937. 22) Gardner, A.: Fibrous dysplasia of the skull with special referance to the regions. Dent Pract Dent Rec 8: 337-345 1963. 14) 古屋光太郎: Fibrous dysplasiaとその類似疾患日整外会誌43: 157-174 1969. 2) 前川厳: 線維性良性骨腫瘍について. fibrous dysplasiaとその類似疾患臨床放射線5: 118-134 1960. 18) 増田正典, 森克己, 他: Fibrous dysplasia of bone. 代謝4: 64-73 1967. 8) Schlumberger, H. G.: fibrous dysplasia of single bones (monostotic fibrous dysplasia). Milit Surg 99: 504-527 1946. 12) Geschickter, C. F. Primary Tumors of the cranial bones. Amer j Cancer 26: 155-180 1936. 26) 立川潤, 市川泰右, 他: 下顎骨に発生したMonostotic fibrous dysplasiaの1例. 日口外誌17: 334-339 1971. 19) Zimmerman, D. C. and Dahlin, D. C.: Fibrous dysplasia of the maxilla and mandible. Oral Surg Oral Med Oral Path 11: 55-68 1958. 5) Weil, F.: 9.Jähriges Mädchen mit pubertas praecox und Knochen brüchigkeit. Wscher 1: 2114-2115 1922. 20) 山本肇, 亀山洋一郎, 他: 線維性骨異形成症の病理組織学的研究 (抄) 口科誌15:149 1966. 23) Wunderer, S.: Die Fibröse dysplasie (Jaffe-Lichtenstein) der Schädelknoschen unter Berücksichtigung der Kiefer. Z Stomat 53: 85-98 1956. 1) Thoma, K. H.: Oral Pathology. 4th Ed. Mosby Co, St. Louis, 1954, p768-791. 3) Mandl, F.: Klinisches und Experimentelles zur Frage der lokalisierten und generalisierten Ostitis fibrosa. Arch f klin chir 143: 245-284 1926. 16) 長谷川秀行, 白川正順, 他: 下顎骨に発生した単骨性線維性骨異形成症の1例日口外誌30: 314-320 1984. 29) 石川梧朗, 秋吉正豊. 口腔病理学II. 増補4刷, 永末書店, 京都, 1977, 972-974頁. 24) 堀越達郎, 工藤逸郎, 他: 線維性骨異形成症と類似疾患の6例. 口科誌18: 785-795 1969. 27) 井上明, 山田哲司, 他: 下顎骨に発生した単骨性線維性骨異形成症の1症例. 日口外誌26: 756-760 1980. 17) Lichtenstein, L. and Jaffe. H. L. Fibrous dysplasia of bone; a condition affecting one, several or many bones, the graver cases of which may present abnormal pigmentation of skin, premature sexual development, hyperthyroidism or still other extraskeletal abnormalities. Arch Path 33: 777-816 1942. 13) Changus, Osteoblastic hyperplasia of bone, A histochemical appraisal of fibrous dysplasia of bone. Cancer 10: 1157-1161 1957. 4) Wieland, E.: Uber Ostitis (richtiger Osteodysplasia) fibrosa cystica congenita. Arch f Kinderh 71: 241-263 1922. 21) Henry, A: Monostotic fibrous dysplasia. J Bone Jt Surg 51-B: 300-306 1969. 25) 稲田嘉孝: 骨腫瘍の診断並びに予後判定に対する血清フォスファターゼ活性度測定の意義の知見補遺. 熊本医会誌37: 522-542 1963. 28) Fries. J. W.: The roentgen features of fibrous dysplasia of the skull and facial bones. A critical analysis of 39 pathologically proved cases. Amer. 1 Roentgenol 77: 71-88 1957. 15) 茂呂茂: 顎骨に生ずる中心性線維性腫瘍ならびに線維性異形成症に関する臨床病理学的研究. 日大歯学41: 389-432 1967. |
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Title | A case of fibrous dysplasia occurred centering in the maxilla and its review of the literature |
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