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Familial Amyloid Polyneuropathy Misdiagnosed as Systemic Sclerosis

dc.contributor.authorAgostinho Pereira, M
dc.contributor.authorLobão, M
dc.contributor.authorMesquita, A
dc.contributor.authorMartins, M
dc.contributor.authorRibeiro, R
dc.date.accessioned2022-02-22T09:51:34Z
dc.date.available2022-02-22T09:51:34Z
dc.date.issued2022
dc.description.abstractWe present the case of a 53-year-old woman of Portuguese ancestry with a diagnosis of progressive systemic sclerosis (SSc), proposed for haematopoietic stem cell transplantation (HSCT). Clinical re-evaluation when assessing eligibility for the procedure led to the alternative diagnosis of familial amyloid polyneuropathy (FAP). We discuss the clinical presentations of FAP and SSc, focusing on their overlapping and distinguishing features. We emphasize the need for a high level of suspicion in order to establish an early diagnosis of FAP in the absence of a family history, and provide prognostic and genetic counselling. Learning points: It is important to review diagnoses, especially when the clinical course is atypical.Cutaneous involvement is a commonly unrecognized feature of familial amyloid polyneuropathy.Hereditary conditions should be included in the differential diagnosis of multisystemic diseases, even in the absence of a family history.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationEur J Case Rep Intern Med. 2022 Jan 18;9(1):003118.pt_PT
dc.identifier.doi10.12890/2022_003118.pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/3970
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherEFIMpt_PT
dc.subjectHSAC MEDpt_PT
dc.subjectHereditarypt_PT
dc.subjectAmyloidosispt_PT
dc.subjectPolyneuropathypt_PT
dc.subjectSclerodermapt_PT
dc.subjectTransthyretin.pt_PT
dc.titleFamilial Amyloid Polyneuropathy Misdiagnosed as Systemic Sclerosispt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.startPage003118pt_PT
oaire.citation.titleEuropean Journal of Case Reports in Internal Medicinept_PT
oaire.citation.volume9pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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