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Presacral malakoplakia presenting as foot drop: a case report.

Yates, TA; Devlin, K; Arnaout, A; Hurt, W; Stone, N; Everett, KV; Pittman, A; Patel, H; Heenan, S; Hart, P; et al. Yates, TA; Devlin, K; Arnaout, A; Hurt, W; Stone, N; Everett, KV; Pittman, A; Patel, H; Heenan, S; Hart, P; Harrison, TS (2023) Presacral malakoplakia presenting as foot drop: a case report. J Med Case Rep, 17 (1). p. 154. ISSN 1752-1947 https://doi.org/10.1186/s13256-023-03883-4
SGUL Authors: Harrison, Thomas Stephen

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Abstract

BACKGROUND: Malakoplakia is a rare condition characterized by inflammatory masses with specific histological characteristics. These soft tissue masses can mimic tumors and tend to develop in association with chronic or recurrent infections, typically of the urinary tract. A specific defect in innate immunity has been described. In the absence of randomized controlled trials, management is based on an understanding of the biology and on case reports. CASE PRESENTATION: Here we describe a case of presacral malakoplakia in a British Indian woman in her late 30s, presenting with complex unilateral foot drop. Four years earlier, she had suffered a protracted episode of intrapelvic sepsis following a caesarean delivery. Resection of her presacral soft tissue mass was not possible. She received empiric antibiotics, a cholinergic agonist, and ascorbic acid. She responded well to medical management both when first treated and following a recurrence of symptoms after completing an initial 8 months of therapy. Whole exome sequencing of the patient and her parents was undertaken but no clear causal variant was identified. CONCLUSIONS: Malakoplakia is uncommon but the diagnosis should be considered where soft tissue masses develop at the site of chronic or recurrent infections. Obtaining tissue for histological examination is key to making the diagnosis. This case suggests that surgical resection is not always needed to achieve a good clinical and radiological outcome.

Item Type: Article
Additional Information: © The Author(s) 2023. Open Access This 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Keywords: Ascorbic acid, Bethanechol, Case report, Ciprofloxacin, Human genetics, Immunopathology, Infectious diseases, Malakoplakia, Peripheral nervous system, Female, Humans, Malacoplakia, Peroneal Neuropathies, Reinfection, Anti-Bacterial Agents, Ascorbic Acid, Humans, Peroneal Neuropathies, Malacoplakia, Ascorbic Acid, Anti-Bacterial Agents, Female, Reinfection, Malakoplakia, Peripheral nervous system, Infectious diseases, Immunopathology, Human genetics, Ciprofloxacin, Bethanechol, Ascorbic acid, Case report, 1199 Other Medical and Health Sciences, General & Internal Medicine
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: J Med Case Rep
ISSN: 1752-1947
Language: eng
Dates:
DateEvent
7 April 2023Published
8 March 2023Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
UNSPECIFIEDNational Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
PubMed ID: 37024963
Web of Science ID: WOS:000963477200004
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/115392
Publisher's version: https://doi.org/10.1186/s13256-023-03883-4

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