Intramandibular plexiform schwannoma presenting as a nonspecific benign lesion: How specific can we be? A case report with a review of the literature

Schwannoma, a benign nerve sheath tumor, is quite rare and more so in jawbones. We report a rare case of a plexiform variant of mandibular schwannoma in a 12-year-old female with a swelling in the left mandible. Clinical features were suggestive of dentigerous cyst as a result of missing premolars and canine. Occlusal and panoramic radiography revealed an osteolytic lesion with scalloping margins, bicortical plate expansion, and agenesis of several teeth. Odontogenic keratocyst, central giant cell granuloma, odontogenic myxoma, and ameloblastic fibroma were given as radiological differential diagnoses. Histopathological examination revealed features of plexiform schwannoma which was given as the final diagnosis. The lesion was treated with surgical excision. Although odontogenic cysts/tumors are often thought of in differential diagnosis whenever well-defined radiolucencies in the jaw are encountered, it is prudent to include schwannoma. This exceptional case adds light to the fact that schwannoma should not be overlooked though it is a rare possibility and must be included in differential diagnosis of odontogenic cysts/tumors

Esophageal Plexiform Schwannoma: A case report / 대한흉부외과학회지

A 39-year-old man presented with a esophageal submucosal tumor on regular check up examination. Preoperative exams showed the typical submucosal tumor as leiomyoma and operative procedure was enucleation for complete resection. Postoperative pathologic diagnosis including histologic and immunohistochemical study was compatible with plexiform schwannoma. Plexiform schwannoma is one of the least common variant of schwannoma that typically shows a plexiform or multinodular pattern. To our knowledge, there is rare case report of plexiform schwannoma originating in the esophagus and we report one case with related literature.

A Case of Multiple Cutaneous Plexiform Schwannomas Accompanying Neurologic Deficits / 대한피부과학회지

Plexiform schwannoma is a rare variant of benign schwannoma characterized by a multinodular and plexiform growth pattern. Schwannomatosis is a recently recognized disorder, defined as multiple, pathologically-proven schwannoma without vestibular tumors, diagnostic of neurofibromatosis 2. Although plexiform schwannoma is usually solitary, multiple plexiform schwannomas do also occur as an isolated finding or in association with neurofibromatosis 2. We describe a 7-year-old girl who had multiple cutaneous plexiform schwannomas and neurologic deficits such as sensorineural hearing loss and amblyopia on her left side. Brain magnetic resonance imaging and ophthalmologic examination was negative for vestibular schwannoma and eye stigmata of neurofibromatosis 2. However, as there is a possibility that the patient may eventually develop additional cranial tumors such as meningiomas or vestibular schwannomas, we therefore recommend that she is periodically screened.

Four Cases of Minocycline-Induced Hyperpigmentation of the Tongue / 대한피부과학회지

Minocycline is a semi-synthetic, broad-spectrum, antimicrobial agent that was first introduced into clinical practice in 1967. Its primary indication is for the treatment of acne vulgaris, where its success has been attributed to a combination of its bacteriostatic and anti-inflammatory activities. There has been recent interest in minocycline use in the treatment of various other chronic inflammatory and immune-mediated diseases such as Behcet's disease and recurrent apthous ulceration. A well-recognized side effect of minocycline treatment is pigmentation, which has been reported in multiple tissues including skin, nail beds, sclera, bone, the thyroid, and teeth. However, pigmentation of the tongue caused by minocycline is very rare. We report four cases of actual pigmented lesions on the tongue and finger nails due to minocycline therapy, followed by a discussion of minocycline-induced hyperpigmentation.

Two Cases of Plexiform Schwannoma / 대한피부과학회지

We present two cases of plexiform schwannoma, a benign peripheral nerve sheath tumor, characterized by a plexiform growth pattern. Plexiform schwannoma must be distinguished from plexiform neurofibroma because of the propensity of the latter for malignant degeneration. Although plexiform schwannoma usually arises sporadically, it can be rarely associated with neurofibromatosis type 2. We report two cases of plexiform schwannoma. One was single sporadic lesion on the abdomen of a 28-year-old woman. The other showed multiple plexiform schwannomas associated with bilateral acoustic neuromas.

Multiple Plexiform Schwannomas Associated with Neurofibromatosis Type 2: A case report

Plexiform schwannoma is a rare benign tumor arising from the peripheral nerve sheath and characterized by a multinodular and plexiform growth pattern. This tumor usually arises sporadically. In rare cases, plexiform schwannomas have been associated with neurofibromatosis type 2. Plexiform schwannoma should be differentiated from plexiform neurofibroma, because the latter is pathognomonic tumor of neurofibromatosis type 1 and has a potential of malignant transformation. We report a case of multiple plexiform schwannomas associated with bilateral acoustic neuromas and meningioma.

A Case of Plexiform Schwannoma / 대한피부과학회지

Plexiform schwannoma is a rare variant of shwannoma, originating from the nerve sheath. It is very impoirtant to differentiate plexiform schwannoma from plexiform neurofibroma, which is pathognomonic of von Reckilnghausen's disease and carries a significant risk of malignant transformation. Plexiform schwannoma is not necessarily associated with von Reckilnghausen's disease and malignant transformation has never been observed. We present a 11-year-old boy who had a nodole on right forearm with tenderness and a tingling sensation. On the histopathological and immunohistochemical examinations, the lesion showed typical features of plexiform schwannoma, The nodule was totally excised under local anesthcsia. Recurrence has not been observed in the six months follow-up period.

Histopathological Analysis of 9 Cases of Plexiform Schwannoma

We present 9 cases of plexiform schwannoma examined at Severance hospital from January, 1980 to September, 1987. The predilection sites of plexiform schwannoma included head and neck including oral cavity. The mean age at the time of diagnosis was 32 years. The difference of sex ratio was not apparent. Histopathological findings revealed multiple round to oval nodules encapsulated by thin fibroconnective tissue with nuclear palisading and Verocay body in each nodule. There was mild to moderate cellular atypia in some area, but mitotic figure was not found. The Bielschowsky's silver stain did not demonstrate any axon within or outside of the nodule. The thin capsule was positive with reticulin stain.