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Primary peripheral T-cell lymphoma of the cervix with mononeuritis multiplex: an unusual case presentation
Peripheral neuropathy (PN) is characterized by the injury to the peripheral nervous system of varied etiology. Lymphoma is one of the etiologies of PN, presenting various neurological manifestations. Neuropathy associated with peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS) is unusua...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hospital Universitário da Universidade de São Paulo
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890812/ https://www.ncbi.nlm.nih.gov/pubmed/35252047 http://dx.doi.org/10.4322/acr.2021.354 |
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author | Seal, Ratul Parkhi, Mayur Kumar, Rajesh Mitra, Suvradeep |
author_facet | Seal, Ratul Parkhi, Mayur Kumar, Rajesh Mitra, Suvradeep |
author_sort | Seal, Ratul |
collection | PubMed |
description | Peripheral neuropathy (PN) is characterized by the injury to the peripheral nervous system of varied etiology. Lymphoma is one of the etiologies of PN, presenting various neurological manifestations. Neuropathy associated with peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS) is unusual and fewer cases are documented in the literature. In addition, PTCL, NOS is extremely rare as primary in the female genital tract, especially uterine cervix, and exhibits aggressive clinical course with poor therapy response. We hereby describe a 47-year-old female who presented with fever and chills for 15 days. Clinical examination revealed left-sided lower motor neuron type of facial nerve palsy with Bell’s phenomenon. Nerve conduction study of all four limbs illustrated asymmetrical axonal neuropathy (motor > sensory), suggesting mononeuritis multiplex. She developed vaginal bleeding during her hospital stay. Pelvic examination and imaging revealed a 4x3cm polypoidal mass on the posterior lip of the cervix, which was excised and diagnosed as extranodal primary PTCL, NOS based on morphology, immunohistochemistry, and in-situ hybridization findings. Besides, the cerebrospinal fluid (CSF) was infiltrated by the lymphoma cells, detected on cell block preparation. The patient succumbed to her illness within one week despite best efforts and the commencement of chemotherapy. No consent was obtainable for nerve biopsy and autopsy. Thus, we report an extremely rare case of primary extranodal PTCL, NOS of the uterine cervix with unusual presentation of mononeuritis multiplex. Further, we discussed the differentials of PTCL, NOS at this extranodal site. |
format | Online Article Text |
id | pubmed-8890812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hospital Universitário da Universidade de São Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-88908122022-03-04 Primary peripheral T-cell lymphoma of the cervix with mononeuritis multiplex: an unusual case presentation Seal, Ratul Parkhi, Mayur Kumar, Rajesh Mitra, Suvradeep Autops Case Rep Clinical Case Report Peripheral neuropathy (PN) is characterized by the injury to the peripheral nervous system of varied etiology. Lymphoma is one of the etiologies of PN, presenting various neurological manifestations. Neuropathy associated with peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS) is unusual and fewer cases are documented in the literature. In addition, PTCL, NOS is extremely rare as primary in the female genital tract, especially uterine cervix, and exhibits aggressive clinical course with poor therapy response. We hereby describe a 47-year-old female who presented with fever and chills for 15 days. Clinical examination revealed left-sided lower motor neuron type of facial nerve palsy with Bell’s phenomenon. Nerve conduction study of all four limbs illustrated asymmetrical axonal neuropathy (motor > sensory), suggesting mononeuritis multiplex. She developed vaginal bleeding during her hospital stay. Pelvic examination and imaging revealed a 4x3cm polypoidal mass on the posterior lip of the cervix, which was excised and diagnosed as extranodal primary PTCL, NOS based on morphology, immunohistochemistry, and in-situ hybridization findings. Besides, the cerebrospinal fluid (CSF) was infiltrated by the lymphoma cells, detected on cell block preparation. The patient succumbed to her illness within one week despite best efforts and the commencement of chemotherapy. No consent was obtainable for nerve biopsy and autopsy. Thus, we report an extremely rare case of primary extranodal PTCL, NOS of the uterine cervix with unusual presentation of mononeuritis multiplex. Further, we discussed the differentials of PTCL, NOS at this extranodal site. Hospital Universitário da Universidade de São Paulo 2022-02-11 /pmc/articles/PMC8890812/ /pubmed/35252047 http://dx.doi.org/10.4322/acr.2021.354 Text en Copyright © 2022 The Author(s). https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Case Report Seal, Ratul Parkhi, Mayur Kumar, Rajesh Mitra, Suvradeep Primary peripheral T-cell lymphoma of the cervix with mononeuritis multiplex: an unusual case presentation |
title | Primary peripheral T-cell lymphoma of the cervix with mononeuritis multiplex: an unusual case presentation |
title_full | Primary peripheral T-cell lymphoma of the cervix with mononeuritis multiplex: an unusual case presentation |
title_fullStr | Primary peripheral T-cell lymphoma of the cervix with mononeuritis multiplex: an unusual case presentation |
title_full_unstemmed | Primary peripheral T-cell lymphoma of the cervix with mononeuritis multiplex: an unusual case presentation |
title_short | Primary peripheral T-cell lymphoma of the cervix with mononeuritis multiplex: an unusual case presentation |
title_sort | primary peripheral t-cell lymphoma of the cervix with mononeuritis multiplex: an unusual case presentation |
topic | Clinical Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890812/ https://www.ncbi.nlm.nih.gov/pubmed/35252047 http://dx.doi.org/10.4322/acr.2021.354 |
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