scholarly journals A treatment case of a pachydrematocele with von Recklinghausen's disease in the mid-face and oral cavity.

1992 ◽  
Vol 38 (7) ◽  
pp. 1167-1175
Author(s):  
Morio TONOGI ◽  
Hiroyasu NOMA ◽  
Akira KATAKURA ◽  
Shinya NAKAJIMA ◽  
Mitsuru YAMA ◽  
...  
1986 ◽  
Vol 32 (6) ◽  
pp. 996-1003 ◽  
Author(s):  
Itaru KOHYA ◽  
Hiroshi TANAKA ◽  
Moriko SAKAMOTO ◽  
Naohiro TAKADA ◽  
Kasumi MATSUSHIMA ◽  
...  

1989 ◽  
Vol 35 (8) ◽  
pp. 2157-2163
Author(s):  
Tomoyuki NAKAGAWA ◽  
Yasuharu TAKENOSHITA ◽  
Shuro KUBO ◽  
Makoto SHIMADA ◽  
Toshio ANDO ◽  
...  

2020 ◽  
Vol 23 (4) ◽  
pp. 6p
Author(s):  
Hossein Danesteh ◽  
Azita Sadeghzade ◽  
Dana Jafarpour

Neurofibroma is a benign tumor which rarely occurs in the oral cavity. Generally, oral neurofibroma is part of a neurofibromatosis type-1 like syndrome (Von Recklinghausen’s disease) and rarely occurs as a solitary lesion of oral cavity. Up to now, few cases have been reported with the solitary neurofibromas of tongue and submandibular gland. The tumor can also be rarely located centrally in the bone. This research presents a central neurofibroma case in the maxillary bone which has no relationship with the neurofibromatosis. Keywords Central neurofibroma; Neurofibromatosis; Solitary neurofibroma; Von Recklinghausen’s disease.


1986 ◽  
Vol 48 (3) ◽  
pp. 491-499
Author(s):  
Shuhei IMAYAMA ◽  
Yutaka YASHIMA ◽  
Atsushi IRIKI ◽  
Emiko SATO ◽  
Harukuni URABE

1987 ◽  
Vol 49 (3) ◽  
pp. 460-464
Author(s):  
Kazumoto KATAGIRI ◽  
Tomohito HONDA ◽  
Satoshi ITAMI ◽  
Etsuji MATSUNAGA ◽  
Hiroshi SHINKAI ◽  
...  

1994 ◽  
Vol 81 (3) ◽  
pp. 362-373 ◽  
Author(s):  
Thomas R. Donner ◽  
Rand M. Voorhies ◽  
David G. Kline

✓ Over a 22-year period, operations were performed on 263 patients for 288 primary benign tumors of major peripheral nerves. The tumors included 85 schwannomas, 197 neurofibromas, and six plexiform neurofibromas. Total removal was achieved in 83 of the 85 schwannomas, and 76 of these patients were available for follow-up evaluation. Motor function either improved or was unchanged in 87% of these patients and 85% of those with pain in the distribution of the involved nerve had either total or partial resolution of their symptoms. Of the neurofibromas, 123 occurred in 121 patients without von Recklinghausen's disease. All tumors within this group were completely excised using a fascicular approach to the tumor. Of the 99 patients available for follow-up evaluation, 90% had either improved or unchanged motor function and 88% had partial or complete resolution of pain syndromes. Fifty-nine patients with von Recklinghausen's disease had 80 tumors removed: 74 fusiform tumors (58 of which were completely removed) and six plexiform tumors. Forty-eight of the 58 patients with gross total removal of fusiform tumors were available for follow-up evaluation, of whom 83% had improved or unchanged motor function and 74% had partial or complete resolution of pain syndromes. All six patients with plexiform tumors had progression of symptoms postoperatively. One brachial plexus schwannoma recurred and was re-excised without subsequent recurrence at the 5-year follow-up evaluation. Several incompletely excised plexiform neurofibromas have recurred with a symptomatic presentation.


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