Cargando…

Malignant peripheral nerve sheath tumour of the oesophagus: a case report

BACKGROUND: Malignant peripheral nerve sheath tumour (MPNST) is a very rare disease, and its pathogenesis is unknown. There are few reports of MPNST of the oesophagus. We report a case of an MPNST that was diagnosed and resected. CASE PRESENTATION: A 30-year-old female presented with dysphagia. She...

Descripción completa

Detalles Bibliográficos
Autores principales: Tomizawa, Kento, Miyazaki, Tatsuya, Yamaguchi, Arisa, Honda, Ryoya, Hoshino, Marie, Yanai, Mitsuhiro, Miyamae, Yohei, Kurosaki, Ryo, Shimizu, Hisashi, Arakawa, Kazuhisa, Ide, Munenori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394979/
https://www.ncbi.nlm.nih.gov/pubmed/32737607
http://dx.doi.org/10.1186/s40792-020-00954-2
_version_ 1783565312810024960
author Tomizawa, Kento
Miyazaki, Tatsuya
Yamaguchi, Arisa
Honda, Ryoya
Hoshino, Marie
Yanai, Mitsuhiro
Miyamae, Yohei
Kurosaki, Ryo
Shimizu, Hisashi
Arakawa, Kazuhisa
Ide, Munenori
author_facet Tomizawa, Kento
Miyazaki, Tatsuya
Yamaguchi, Arisa
Honda, Ryoya
Hoshino, Marie
Yanai, Mitsuhiro
Miyamae, Yohei
Kurosaki, Ryo
Shimizu, Hisashi
Arakawa, Kazuhisa
Ide, Munenori
author_sort Tomizawa, Kento
collection PubMed
description BACKGROUND: Malignant peripheral nerve sheath tumour (MPNST) is a very rare disease, and its pathogenesis is unknown. There are few reports of MPNST of the oesophagus. We report a case of an MPNST that was diagnosed and resected. CASE PRESENTATION: A 30-year-old female presented with dysphagia. She had been aware of the dysphagia approximately 6 months before presentation. The chest X-ray showed shadows in the right mediastinum. Barium fluoroscopy revealed a semicircular raised lesion in the lower oesophagus. Upper gastrointestinal endoscopy revealed a type 1 oesophageal tumour centred on the posterior wall 26–35 cm from the incisors. The surface was ulcerated, and the tumour was exposed. The affected area showed no iodine uptake. The EUS showed an isoechoic mass. The CT scan showed a mass of 71 × 61 × 55 mm in the beginning of the lower oesophagus with low density mass and swelling of the right recurrent nerve lymph node to 12 mm. On FDG-PET, the tumour showed an SUVmax of 11.05, and no abnormal accumulation was found in lymph nodes or other organs. The MRI showed a hyperintense mass on the T2WI, which had prolonged contrast enhancement, and no findings of invasion into surrounding tissue were found. The patient underwent right thoracotomy and open thoracic oesophagectomy. The affected lymph node was tumour negative by rapid pathological diagnosis during the operation. Histologically, spindle cells with different-sized nuclei were mixed throughout the tissue. Some regions showed nuclear polymorphism or a storiform pattern, and locally, there were approximately 7 mitoses/10 HPFs. The margin was relatively clear, but spindle-shaped tumour cells infiltrated the surrounding interstitium and basal myoepithelium, and the patient was diagnosed with MPNST. In this case, the postoperative course was good, and 16 months after the operation, the patient is currently under observation at the outpatient stage without recurrence. CONCLUSIONS: MPNST in the oesophagus is a relatively rare disease. Diagnosis before treatment is sometimes difficult, but the prognosis is good if radical resection is possible.
format Online
Article
Text
id pubmed-7394979
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-73949792020-08-18 Malignant peripheral nerve sheath tumour of the oesophagus: a case report Tomizawa, Kento Miyazaki, Tatsuya Yamaguchi, Arisa Honda, Ryoya Hoshino, Marie Yanai, Mitsuhiro Miyamae, Yohei Kurosaki, Ryo Shimizu, Hisashi Arakawa, Kazuhisa Ide, Munenori Surg Case Rep Case Report BACKGROUND: Malignant peripheral nerve sheath tumour (MPNST) is a very rare disease, and its pathogenesis is unknown. There are few reports of MPNST of the oesophagus. We report a case of an MPNST that was diagnosed and resected. CASE PRESENTATION: A 30-year-old female presented with dysphagia. She had been aware of the dysphagia approximately 6 months before presentation. The chest X-ray showed shadows in the right mediastinum. Barium fluoroscopy revealed a semicircular raised lesion in the lower oesophagus. Upper gastrointestinal endoscopy revealed a type 1 oesophageal tumour centred on the posterior wall 26–35 cm from the incisors. The surface was ulcerated, and the tumour was exposed. The affected area showed no iodine uptake. The EUS showed an isoechoic mass. The CT scan showed a mass of 71 × 61 × 55 mm in the beginning of the lower oesophagus with low density mass and swelling of the right recurrent nerve lymph node to 12 mm. On FDG-PET, the tumour showed an SUVmax of 11.05, and no abnormal accumulation was found in lymph nodes or other organs. The MRI showed a hyperintense mass on the T2WI, which had prolonged contrast enhancement, and no findings of invasion into surrounding tissue were found. The patient underwent right thoracotomy and open thoracic oesophagectomy. The affected lymph node was tumour negative by rapid pathological diagnosis during the operation. Histologically, spindle cells with different-sized nuclei were mixed throughout the tissue. Some regions showed nuclear polymorphism or a storiform pattern, and locally, there were approximately 7 mitoses/10 HPFs. The margin was relatively clear, but spindle-shaped tumour cells infiltrated the surrounding interstitium and basal myoepithelium, and the patient was diagnosed with MPNST. In this case, the postoperative course was good, and 16 months after the operation, the patient is currently under observation at the outpatient stage without recurrence. CONCLUSIONS: MPNST in the oesophagus is a relatively rare disease. Diagnosis before treatment is sometimes difficult, but the prognosis is good if radical resection is possible. Springer Berlin Heidelberg 2020-07-31 /pmc/articles/PMC7394979/ /pubmed/32737607 http://dx.doi.org/10.1186/s40792-020-00954-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Case Report
Tomizawa, Kento
Miyazaki, Tatsuya
Yamaguchi, Arisa
Honda, Ryoya
Hoshino, Marie
Yanai, Mitsuhiro
Miyamae, Yohei
Kurosaki, Ryo
Shimizu, Hisashi
Arakawa, Kazuhisa
Ide, Munenori
Malignant peripheral nerve sheath tumour of the oesophagus: a case report
title Malignant peripheral nerve sheath tumour of the oesophagus: a case report
title_full Malignant peripheral nerve sheath tumour of the oesophagus: a case report
title_fullStr Malignant peripheral nerve sheath tumour of the oesophagus: a case report
title_full_unstemmed Malignant peripheral nerve sheath tumour of the oesophagus: a case report
title_short Malignant peripheral nerve sheath tumour of the oesophagus: a case report
title_sort malignant peripheral nerve sheath tumour of the oesophagus: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394979/
https://www.ncbi.nlm.nih.gov/pubmed/32737607
http://dx.doi.org/10.1186/s40792-020-00954-2
work_keys_str_mv AT tomizawakento malignantperipheralnervesheathtumouroftheoesophagusacasereport
AT miyazakitatsuya malignantperipheralnervesheathtumouroftheoesophagusacasereport
AT yamaguchiarisa malignantperipheralnervesheathtumouroftheoesophagusacasereport
AT hondaryoya malignantperipheralnervesheathtumouroftheoesophagusacasereport
AT hoshinomarie malignantperipheralnervesheathtumouroftheoesophagusacasereport
AT yanaimitsuhiro malignantperipheralnervesheathtumouroftheoesophagusacasereport
AT miyamaeyohei malignantperipheralnervesheathtumouroftheoesophagusacasereport
AT kurosakiryo malignantperipheralnervesheathtumouroftheoesophagusacasereport
AT shimizuhisashi malignantperipheralnervesheathtumouroftheoesophagusacasereport
AT arakawakazuhisa malignantperipheralnervesheathtumouroftheoesophagusacasereport
AT idemunenori malignantperipheralnervesheathtumouroftheoesophagusacasereport