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Progressive cranial neuropathy and uterine involvement in myeloid sarcoma

A rare extramedullary manifestation of haematological malignancy, myeloid sarcoma is most commonly seen in patients with acute myeloid leukaemia. We report on an adult patient who presented with an atypical phenotype of progressive cranial neuropathy without blood or bone marrow involvement, and in...

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Autores principales: Khoo, Anthony, Kimber, Thomas, Cohen, Penelope, Ghaoui, Roula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871711/
https://www.ncbi.nlm.nih.gov/pubmed/33681768
http://dx.doi.org/10.1136/bmjno-2019-000006
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author Khoo, Anthony
Kimber, Thomas
Cohen, Penelope
Ghaoui, Roula
author_facet Khoo, Anthony
Kimber, Thomas
Cohen, Penelope
Ghaoui, Roula
author_sort Khoo, Anthony
collection PubMed
description A rare extramedullary manifestation of haematological malignancy, myeloid sarcoma is most commonly seen in patients with acute myeloid leukaemia. We report on an adult patient who presented with an atypical phenotype of progressive cranial neuropathy without blood or bone marrow involvement, and in whom obtaining material for pathological diagnosis was made challenging by unusual findings of absent fluorodeoxyglucose-positron emission tomography avidity and involvement of sites not readily accessible to biopsy (orbital apex and cauda equina). The eventual diagnosis was obtained through biopsy of the uterine cervix before being verified on repeat lymph node and cerebrospinal fluid sampling prior to initiation of chemotherapy.
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spelling pubmed-78717112021-03-04 Progressive cranial neuropathy and uterine involvement in myeloid sarcoma Khoo, Anthony Kimber, Thomas Cohen, Penelope Ghaoui, Roula BMJ Neurol Open Short Report A rare extramedullary manifestation of haematological malignancy, myeloid sarcoma is most commonly seen in patients with acute myeloid leukaemia. We report on an adult patient who presented with an atypical phenotype of progressive cranial neuropathy without blood or bone marrow involvement, and in whom obtaining material for pathological diagnosis was made challenging by unusual findings of absent fluorodeoxyglucose-positron emission tomography avidity and involvement of sites not readily accessible to biopsy (orbital apex and cauda equina). The eventual diagnosis was obtained through biopsy of the uterine cervix before being verified on repeat lymph node and cerebrospinal fluid sampling prior to initiation of chemotherapy. BMJ Publishing Group 2019-11-13 /pmc/articles/PMC7871711/ /pubmed/33681768 http://dx.doi.org/10.1136/bmjno-2019-000006 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Short Report
Khoo, Anthony
Kimber, Thomas
Cohen, Penelope
Ghaoui, Roula
Progressive cranial neuropathy and uterine involvement in myeloid sarcoma
title Progressive cranial neuropathy and uterine involvement in myeloid sarcoma
title_full Progressive cranial neuropathy and uterine involvement in myeloid sarcoma
title_fullStr Progressive cranial neuropathy and uterine involvement in myeloid sarcoma
title_full_unstemmed Progressive cranial neuropathy and uterine involvement in myeloid sarcoma
title_short Progressive cranial neuropathy and uterine involvement in myeloid sarcoma
title_sort progressive cranial neuropathy and uterine involvement in myeloid sarcoma
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871711/
https://www.ncbi.nlm.nih.gov/pubmed/33681768
http://dx.doi.org/10.1136/bmjno-2019-000006
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