Plexiform schwannoma involving the trachea and recurrent laryngeal nerve: a case report
© Nagata et al. 2015
Received: 26 May 2015
Accepted: 12 August 2015
Published: 25 August 2015
Plexiform schwannoma is an infrequent variant of schwannoma characterized grossly and microscopically by multi-nodular growth. Although plexiform schwannoma has such growth patterns, it is a benign tumor as well as a conventional schwannoma. It rarely infiltrates adjacent organs or arises from the organ itself. In this report, we describe a case in which plexiform schwannoma involved the tracheal wall and left recurrent laryngeal nerve to a great extent. As it was expected to be difficult to achieve complete resection even if the longer tracheal resection were performed, we preserved the trachea and resected as much of the tumor as possible. This report is thought to be the first to describe plexiform schwannoma infiltrating or growing from the trachea. Although the treatment decisions we made might be controversial, we believed we could make an accurate diagnosis and adequate treatment decision through surgery.
KeywordsTracheal tumor Mediastinal tumor Plexiform schwannoma
Plexiform schwannoma is an infrequent variant of schwannoma characterized grossly and microscopically by multinodular growth . Although plexiform schwannoma has such growth patterns, it is a benign tumor as well as a conventional schwannoma. It rarely infiltrates adjacent organs or arises from the organ itself. In this report, we describe a case in which plexiform schwannoma involved the tracheal wall and left recurrent laryngeal nerve to a great extent. This is thought to be the first case report of plexiform schwannoma infiltrating or growing from the trachea.
The pathological features were identical to those of typical schwannomas, including being composed solely of Schwann cells frequently disposed in a compact, palisaded fashion (Antoni A) (Fig. 3b) and occasionally in a loose texture (Antoni B). This tumor did not have cellular atypia, hyperchromasia either. Cellularity was not high. There was no remarkable pleomorphism. We could confirm few mitotic activities. Immunohistological staining for S-100 protein showed diffuse positivity, while that for neurofilament showed weak positivity only in peripheral areas, which is atypical for a neurofibroma. The patient’s postoperative course was uneventful. A lump on the trachea remained, but no further growth was observed in an 8-month postoperative follow-up period.
Taking the findings for this tumor into consideration, we can postulate two hypotheses about how this plexiform schwannoma progressed. First, it is possible that there were two individual tumors—one arising from the left recurrent laryngeal nerve and the other from the trachea itself. Second, the plexiform schwannoma may have originated from the recurrent nerve and infiltrated the tracheal wall. Whichever postulation is true, such an occurrence is very rare.
Plexiform schwannomas have been reported to represent 4.3 % of all schwannomas, and they are often seen in the head and neck region . Only one case of tracheal plexiform schwannoma was described in a case series reporting uncommon primary tracheal tumors , and it was not presented in detail. In a literature search using PubMed, we could not find any description of a plexiform schwannoma originating from the recurrent laryngeal nerve or of a plexiform schwannoma infiltrating the tracheal wall. In one report, the association of plexiform schwannoma with neurofibromatosis type 2 and with schwannomatosis was 5 % each . Our patient did not have a history of bilateral vestibular schwannomas or of tumors arising from the central nervous system, such as meningiomas. He also did not have a family history suggesting neurofibromatosis. Schwannomatosis has recently been recognized as the third major form of neurofibromatosis that causes multiple schwannomas without a diagnosis of neurofibromatosis type 2 . Some researchers have reported genetic alterations in this disorder . However, the diagnostic criteria have not yet been established. Our patient had a history of left eyelid schwannoma, and he may be diagnosed with schwannomatosis in the future.
If repeated needle biopsies or resection of the intraluminal bulge under rigid bronchoscopy had proven schwannoma before surgery, we might avoid trying the risky tracheal resection and observe the tumor unless tumor growing or tracheal stenosis occurred. However, at that time, it was not expected that the tumor was a benign tumor, such as schwannoma, and a repeat biopsy was not done. We therefore determined that we could make an accurate diagnosis and adequate treatment decision through surgery. After the intraoperative diagnosis, we determined to preserve the trachea and resect as much of the tumor as possible. Wright and coworkers argued that tracheal resection by more than 4 cm was a significant risk factor for anastomotic complications, although there were some measures to loosen the tension . In the present case, even if we had attempted the longer tracheal resection, there would be no guarantee that we would not leave a tumor at the tracheal stump. Residual plexiform schwannoma can recur. Recurrent plexiform schwannomas were reported even with such a high-risk surgery [6, 7]. Moreover, as the tumor had infiltrated a part of the esophageal wall, we considered that it would be impossible to achieve curative resection. Plexiform schwannoma can become enlarged, but it occurs slowly. Debulking is supposed to extend significantly the progression-free period. Periodic follow-up must continue in order to check for regrowth. If this tumor grows up intraluminally, we will resect it under rigid bronchoscopy.
Pathological diagnosis of this tumor was typical schwannoma without malignant findings. Some of plexiform schwannoma are difficult to be differentiated from malignant peripheral nerve sheath tumor . With detailed pathological findings about cellularity and mitotic activity, this tumor could clearly be distinguished from malignancy. Therefore, the prognosis of this case is expected to be good though local recurrence may happen. A few malignant transformations were reported in familial schwannomatosis . It is unknown whether the plexiform schwannoma in this patient may transform to the malignancy. We should suspect of malignant transformation when we see the rapid enlargement.
We experienced an extremely rare case of plexiform schwannoma involving the tracheal wall and left recurrent nerve to a great extent. Appropriate treatment was difficult to determine. Periodic follow-up must continue in order to check for regrowth.
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