Journal Information
Vol. 102. Issue 4.
(1 April 2025)
Images in Paediatrics
Full text access
Difficulty in raising the arm: Parsonage-Turner syndrome
Dificultad para elevar el brazo: síndrome de Parsonage-Turner
Visits
642
Violeta Martí Enrique
Corresponding author
marti_vio@gva.es

Corresponding author.
, Joaquín López Cruz, José María Olmos García, Fátima Pareja Marín
Hospital Mare de Déu dels Lliris, Alcoi, Alicante, Spain
This item has received
Article information
Full Text
Bibliography
Download PDF
Statistics
Figures (3)
Show moreShow less
Full Text

A boy aged 5 years presented with left upper extremity (LUE) dysfunction of three weeks’ duration. No history of trauma preceding the onset. The week before, he had experienced an episode of acute bronchitis.

The salient findings in the examination were the inability to raise the LUE and pain on palpation of the left shoulder; unexpectedly, the patient experienced no pain at rest (Fig. 1). Weakness in the left forearm and hand. The rest of the physical examination was normal.

Figure 1.

Physical examination. Marked limitation of LUE abduction. Suspected involvement of rotator cuff and deltoid muscles and musculocutaneous nerve (C5–C6).

(0.04MB).

The evaluation included a blood panel, serologic tests for infectious agents, nasopharyngeal aspiration, radiography, an ultrasound scan of the LUE and lumbar puncture, with no relevant findings.

An MRI scan of the head and spine was performed and, due to the unremarkable findings, followed by an MRI scan of the affected area, which revealed edema at the level of the muscles of the rotator cuff and brachial plexus hyperintensity (Fig. 2).

Figure 2.

MRI with STIR hyperintensity at the level of the left brachial plexus trunks (A and B), with no discontinuity or associated masses, and signs of acute denervation with mild edema at the supraspinatus and infraspinatus muscles. Normal thickness and signal intensity in cervical spinal cord, with no evidence of space-occupying lesions in the spinal canal. Normal morphology, alignment and signal intensity in vertebral bodies, posterior elements and intervertebral discs.

(0.03MB).

Nerve conduction studies of the LUE evinced left-sided acute pan brachial plexopathy with greater involvement of the upper trunk and axonotmesis in the median and distal ulnar nerves with reduced axonal amplitude. The needle electrode examination was inconclusive, with absence of fibrillation and fasciculation potentials (Fig. 3).

Figure 3.

(C) The motor nerve conduction study assessed the axillary (B), musculocutaneous, median (A) and ulnar nerves on both sides, with stimulation at Erb point, arm, elbow and wrist, with recording electrodes placed at the deltoid, biceps, abductor pollicis brevis and abductor digiti minimi muscles, showing a late response of the median nerve to stimulation of Erb point. (D) The sensory nerve conduction study assessed the left median nerve at the level of the third digit and the left ulnar nerve at the level of the fifth digit. We obtained reduced amplitude values in the normal range on distal stimulation at the wrist, and significant reduction on stimulation at the elbow (axonal degeneration reached the elbow, but not the wrist). The electrophysiological findings were compatible with acute left pan brachial plexopathy with predominant involvement of the upper trunk and axonotmesis of the median and distal ulnar nerves.

(0.29MB).

The combination of electrodiagnostic, clinical and magnetic resonance features were compatible with Parsonage-Turner sydrome,1 a disease that is rare in the pediatric age group.2

The patient started rehabilitation and treatment with oral anti-inflamatories,3 and has exhibited progressive, albeit slow, improvement to date (one year of follow-up).

References
[1]
A.J. Cepillo Boluda, M. Mayordomo Almendros, I. Onsurbe Ramírez, D. Toledo León, O. García Mialdea, M.P. Martín-Tamayo Blázquez.
Una rareza infradiagnosticada: síndrome de Parsonage-Turner (neuritis braquial aguda).
Rev Pediatr Aten Primaria, 14 (2012), pp. 145-148
[2]
J. IJspeert, R. Janssen, N. van Alfen.
Neuralgic amyotrophy.
Curr Opin Neurol, 34 (2021), pp. 605-612
[3]
E. Rotondo, N. Pellegrino, C. Di Battista, A. Graziosi, V. Di Stefano, P. Striano.
Clinico-diagnostic features of neuralgic amyotrophy in childhood.
Neurol Sci, 41 (2020), pp. 1735-1740
Copyright © 2024. Asociación Española de Pediatría
Download PDF
Idiomas
Anales de Pediatría (English Edition)
Article options
Tools