Inclusion body myopathy (Q41418): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A miopatia por corpos de inclusão (MCI) é diferenciada da polimiosite (PM) e dermatomiosite (DM) com base nas características clínicas e histopatológicas. Um fenótipo clínico típico é caracterizado por início insidioso de fraqueza muscular ao longo de meses a anos, fraqueza muscular localizada predominantemente nos músculos da coxa e flexores dos dedos e resistência ao tratamento com glicocorticoides. As características histopatológicas típicas incluem inclusões sarcoplasmáticas e nucleares, e vacúolos com bordas.
@@ description / en / description / en @@
+Inclusion body myopathy (IBM) is distinguished from polymyositis (PM) and dermatomyositis (DM) on the basis of clinical and histopathological features. A characteristic clinical phenotype is characterised by insidious onset of muscle weakness over months to years, muscle weakness localised predominantly in the thigh muscles and finger flexors, and resistance to glucocorticoid treatment. Typical histopathologic features include sarcoplasmic and nuclear inclusions and rimmed vacuoles.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/983668658
@@ Property / Canonical URI: https://id.who.int/icd/entity/983668658 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:4A41.2
@@ Property / CURIE: CID11:4A41.2 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-4A41.2
@@ Property / Canary Token: dki-india-4A41.2 / 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 @@
+G72.8
@@ Property / Linked ICD 10: G72.8 / rank @@
+Normal rank

Latest revision as of 07:35, 13 August 2026

Inclusion body myopathy (IBM) is distinguished from polymyositis (PM) and dermatomyositis (DM) on the basis of clinical and histopathological features. A characteristic clinical phenotype is characterised by insidious onset of muscle weakness over months to years, muscle weakness localised predominantly in the thigh muscles and finger flexors, and resistance to glucocorticoid treatment. Typical histopathologic features include sarcoplasmic and nuclear inclusions and rimmed vacuoles.

Language	Label	Description	Also known as
default for all languages	4A41.2
English	Inclusion body myopathy	Inclusion body myopathy (IBM) is distinguished from polymyositis (PM) and dermatomyositis (DM) on the basis of clinical and histopathological features. A characteristic clinical phenotype is characterised by insidious onset of muscle weakness over months to years, muscle weakness localised predominantly in the thigh muscles and finger flexors, and resistance to glucocorticoid treatment. Typical histopathologic features include sarcoplasmic and nuclear inclusions and rimmed vacuoles.