Autoimmune myopathy (Q41407): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A miopatia autoimune é um subgrupo de miopatias inflamatórias idiopáticas que, apesar de terem diversas causas, apresentam as características histopatológicas comuns de necrose de miócitos sem inflamação significativa. Os pacientes apresentam uma miopatia proximal simétrica grave subaguda, associada a um nível de creatinoquinase acentuadamente elevado. Eles são mais provavelmente imunomediados, pois respondem à imunoterapia. É frequentemente acompanhada por terapia com estatinas, doenças do tecido conjuntivo, câncer e autoanticorpos específicos para partícula de reconhecimento de sinal (SRP) ou 3-hidroxi-3-metilglutaril-coenzima A redutase (HMGCR).
@@ description / en / description / en @@
+Autoimmune myopathy is a subgroup of idiopathic inflammatory myopathies, which, despite diverse causes, have the common histopathological features of myocyte necrosis without significant inflammation. Patients present with a subacute severe symmetrical proximal myopathy, associated with a markedly elevated creatine kinase level. These are most likely immune-mediated, as they respond to immunotherapy. It is often accompanied by statin therapy, connective tissue diseases, cancer, and autoantibodies specific for signal recognition particle (SRP) or 3-hydroxy-3-methylglutaryl–coenzyme A reductase (HMGCR).
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1227790808
@@ Property / Canonical URI: https://id.who.int/icd/entity/1227790808 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:8C81
@@ Property / CURIE: CID11:8C81 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-8C81
@@ Property / Canary Token: dki-india-8C81 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank
@@ Property / Linked ICD 10 @@
+G72
@@ Property / Linked ICD 10: G72 / rank @@
+Normal rank

Latest revision as of 07:34, 13 August 2026

Autoimmune myopathy is a subgroup of idiopathic inflammatory myopathies, which, despite diverse causes, have the common histopathological features of myocyte necrosis without significant inflammation. Patients present with a subacute severe symmetrical proximal myopathy, associated with a markedly elevated creatine kinase level. These are most likely immune-mediated, as they respond to immunotherapy. It is often accompanied by statin therapy, connective tissue diseases, cancer, and autoantibodies specific for signal recognition particle (SRP) or 3-hydroxy-3-methylglutaryl–coenzyme A reductase (HMGCR).

Language	Label	Description	Also known as
default for all languages	8C81
English	Autoimmune myopathy	Autoimmune myopathy is a subgroup of idiopathic inflammatory myopathies, which, despite diverse causes, have the common histopathological features of myocyte necrosis without significant inflammation. Patients present with a subacute severe symmetrical proximal myopathy, associated with a markedly elevated creatine kinase level. These are most likely immune-mediated, as they respond to immunotherapy. It is often accompanied by statin therapy, connective tissue diseases, cancer, and autoantibodies specific for signal recognition particle (SRP) or 3-hydroxy-3-methylglutaryl–coenzyme A reductase (HMGCR).