Man in a Barrel Syndrome

Earn CME/CE in your profession:


Continuing Education Activity

Man in a barrel syndrome is a neurological syndrome involving bilateral upper extremity weakness with preserved facial and lower extremity strength. This syndrome can result from injury to the bilateral cerebral hemispheres, the cervical spinal cord, or bilateral brachial plexuses. This activity reviews the evaluation and management of man in a barrel syndrome and highlights the role of the interprofessional team in evaluating and treating patients with this condition.

Objectives:

  • Describe the pathophysiology of man in a barrel syndrome.
  • Summarize the localization of neurologic lesions that can cause a man in a barrel syndrome.
  • Describe the typical imaging findings associated with man in a barrel syndrome.
  • Describe the importance of collaboration and communication amongst the interprofessional team to enhance the delivery of care for patients affected by a man in a barrel syndrome.

Introduction

Man in a barrel syndrome (MIBS) is a neurologic syndrome characterized by weakness in the bilateral upper extremities (brachial diplegia) with preserved strength in the face, neck, and bilateral lower extremities.

Clinically a patient appears as though they are "stuck in a barrel" with impaired bilateral arm movement and normal facial, cervical, and lower extremity strength.

MIBS can result from bilateral symmetric injury to the brain affecting motor fibers that control arm movement and can also occur following injury to the brainstem, cervical spinal cord, bilateral brachial plexus, or peripheral nerves.

Systemic hypotension causing bilateral watershed strokes is a common cause of MIBS. Watershed strokes occur between the "border zones" of the cerebral vascular territories. When blood pressure is low to the point that it is insufficient to supply blood flow to the most distal arterial small vessel branches, these "border zones" do not receive enough oxygenated blood to survive, resulting in cell death. Cardiac arrest, causing impaired blood flow to the brain, can cause MIBS.[1]

Etiology

Man in a barrel syndrome can result from bilateral watershed strokes due to systemic hypotension, such as seen in cardiac arrest.

  • The internal carotid artery supplies blood flow to the anterior two-thirds of the brain via the anterior cerebral artery (ACA) and the middle cerebral artery (MCA). The most distal branches of the ACA and MCA supply brain tissue, including upper extremity motor fibers. In the setting of inadequate blood flow to both sides, the brain, these most distal branches, or watershed zones, do not receive an adequate amount of oxygenated blood, resulting in the death of these cells. Based on the neuroanatomy of these anterior circulation watershed zones, damage to these areas can result in bilateral upper extremity weakness.[2]
  • Any lesion affecting the bilateral upper extremity motor fibers can result in similar clinical findings of bilateral upper extremity weakness - including hemorrhage, inflammatory lesions, traumatic injury, or neoplastic or metastatic disease.[3]
  • Acute ischemia in the brainstem pyramidal decussation or cervical spinal cord, compressive or intrinsic cervical spinal cord lesions affecting upper extremity motor fibers while sparing lower extremity motor fibers, and peripheral neuropathic injury involving the bilateral nerve roots, brachial plexus, peripheral nerves, or neuromuscular junction can all result in MIBS.[4][5]

Epidemiology

Man in a barrel syndrome is a rare syndrome, and the exact incidence is unknown. MIBS affects men and women equally. Cerebral hypoperfusion causing bilateral watershed strokes is a common cause of MIBS.[6] Watershed strokes make up an estimated 10% of all ischemic strokes.[7]

Pathophysiology

Man in a barrel syndrome results from damage to the bilateral upper extremity motor fibers, sparing the bilateral lower extremity motor fibers. Bilateral symmetric damage isolated to the upper extremity motor fibers in the motor cortex, corona radiata, internal capsule, basal ganglia, brainstem, anterior spinal cord, cervical nerve roots, brachial plexus, peripheral nerves, or neuromuscular junction can result in MIBS. Damage to the anterior horn cells, such as in HTLV-1 or amyotrophic lateralizing sclerosis, can also present with bilateral upper extremity weakness.[8][9]

History and Physical

Evaluation with a detailed history and neurologic examination in which bilateral arm strength is impaired and bilateral cervical, facial, and leg strength is preserved are the first steps in diagnosing man in a barrel syndrome.

Neurologic examination in a patient with MIBS is significant for weakness in the bilateral upper extremities and preserved strength in the bilateral neck and lower extremities.

  • Depending on the location of the neurologic injury, the mental status may be normal to severely impaired.
  • In patients with a central nervous system injury such as stroke or a cervical spine lesion causing MIBS, reflexes are commonly brisk, whereas, in a peripheral nervous system dysfunction causing MIBS such as multifocal motor neuropathy, myasthenia gravis, or bilateral brachial plexus injuries, reflexes are diminished or absent.[10]

Once the clinical diagnosis of MIBS is made based on the neurologic exam, the next step is to localize the causative lesion(s).

  • History may suggest the location of the injury; for example, MIBS following a cardiac arrest with prolonged time without a pulse suggests bilateral watershed strokes, whereas a recent neck injury suggests a cervical spine lesion or bilateral upper extremity injury suggests bilateral brachial plexus injury.
  • Recent surgery with the traction of the arms can suggest a bilateral brachial plexopathy.[11][12][1]

Evaluation

Once the clinical diagnosis of MIBS is made, the next step is to localize the lesion(s), causing bilateral upper extremity weakness.

  • Brain imaging with magnetic resonance imaging (MRI) or computed tomography (CT) can identify intracranial ischemic, hemorrhagic, metastatic, or inflammatory lesions. Cervical spine imaging with CT can identify and compressive cervical spine lesion, and MRI of the cervical spine can localize any extrinsic compressive or intrinsic lesion in the cervical spine.
  • If the brain and cervical spine imaging do not reveal a cause of MIBS, the brachial plexuses should be evaluated, MRI can identify injury to the brachial plexus, and electromyography (EMG) / nerve conduction studies can identify the location of the nerve root, brachial plexus or peripheral nerve dysfunction.
  • Watershed stroke is the most common cause of MIBS; for patients with watershed stroke, imaging of the cervicocephalic arterial vasculature should be performed to evaluate for any flow-limiting stenoses. If significant flow-limiting stenoses are found in the internal carotid arteries, revascularization with carotid endarterectomy or stent placement may be beneficial to reduce the risk of subsequent stroke.[13]

Treatment / Management

Treatment for man in a barrel syndrome varies dependent upon the location and type of neurologic injury.

  • For patients with watershed stroke, treatment includes maintaining adequate blood pressure to prevent extension of stroke, evaluation for any arterial stenosis which may have predisposed to hypoperfusion, initiation of antithrombotic medication, and correction of the underlying abnormality causing hypotension.
  • For compressive cervical spine lesions, emergent surgical decompression should be considered. Intrinsic cervical spinal inflammatory conditions can be treated with steroids. Physical therapy and occupational therapy treatment are important to help improve functional recovery in man in a barrel syndrome.

Differential Diagnosis

The differential diagnosis for man in a barrel syndrome includes the following lesions along the neuroaxis:

  1. Bilateral cerebral upper extremity motor fibers (watershed ischemic stroke, hemorrhagic, traumatic injury, inflammatory, metastatic disease) 
  2. Cervical spine (external compressive lesion, ischemia, inflammatory or infectious process) 
  3. Bilateral brachial plexus (mechanical injury, inflammatory)
  4. Peripheral neuropathic process (toxic or metabolic neuropathy, inflammatory, auto-immune such as multifocal motor neuropathy or myasthenia gravis)

Prognosis

The prognosis for man in a barrel syndrome depends on the type and location of the lesion(s). The prognosis for recovery from bilateral watershed strokes is variable depending on the extent of ischemic damage. In comatose patients with MIBS following extensive watershed strokes, survival is less than 10%.[6] Bilateral intracerebral hemorrhage tends to have a poor prognosis but depends on the extent of tissue damage. Recovery from cervical spine compressive lesions depends on how quickly the lesion is identified and surgically decompressed. MIBS due to myasthenia gravis can be fully reversible with treatment of myasthenia.[14]

Complications

Complications from bilateral intracerebral injury can include cognitive deficits, sensory loss, language dysfunction, weakness, and spasticity. Cervical spinal cord injury complications include weakness, sensory loss, spasticity and bowel, and bladder dysfunction. Bilateral brachial plexus injury complications include motor and sensory deficits in the bilateral upper extremities.

Consultations

Neurologist consultation to perform a detailed neurologic examination and localize the lesion is the first step in evaluating bilateral arm weakness. Radiologist interpretation of brain and cervical spine imaging to identify the etiology of the causative lesion should be performed. A neurosurgeon may be consulted if the lesion is amenable to surgical intervention, such as a brain tumor or a compressive cervical spinal lesion. Physical therapy, occupational therapy, and physiatry collaborate to design and implement a rehabilitation plan to improve motor function.

Deterrence and Patient Education

Patients with MIBS should be counseled on the underlying etiology of MIBS, whether it may be a stroke, tumor, metastatic, auto-immune, or inflammatory disease, and appropriate treatment.

Pearls and Other Issues

Man in a barrel syndrome is a rare neurologic syndrome involving bilateral upper extremity weakness with preserved neck and lower extremity strength that is important to identify quickly as localization of the lesion(s) causing weakness may be reversible. Bilateral cerebral or cervical spinal lesions are the most common causes of MIBS, although various peripheral neuropathic processes have also been described.

Enhancing Healthcare Team Outcomes

Interprofessional team coordination is crucial to identify and treat a person with a man in a barrel syndrome. This interprofessional team includes clinicians (MDs, DOs, NPs, and PAs), specialists (primarily neurologists), nurses, and physical or occupational therapists. A detailed history and physical examination by a provider can diagnose MIBS. Radiology technicians and radiologists are integral in identifying the etiology of the underlying causative lesion. Neurosurgery may be necessary for tumors or compressive cervical spine lesions, causing MIBS. Once the underlying lesion is treated, an interprofessional rehabilitation team can help the patient on the road to functional recovery. A coordinated effort from all interprofessional team members with open information sharing about the patient's case will drive the best possible outcomes. [Level 5]


Details

Author

Jeffrey Bodle

Updated:

6/12/2023 8:01:30 PM

References


[1]

Shaw PJ, Tharakaram S, Mandal SK. Brachial diplegia as a sequel to cardio-respiratory arrest: 'man-in-the-barrel syndrome'. Postgraduate medical journal. 1990 Sep:66(779):788     [PubMed PMID: 2235821]


[2]

Sasaki R, Yamashita T, Tadokoro K, Matsumoto N, Nomura E, Omote Y, Takemoto M, Hishikawa N, Ohta Y, Abe K. Direct arterial damage and neurovascular unit disruption by mechanical thrombectomy in a rat stroke model. Journal of neuroscience research. 2020 Oct:98(10):2018-2026. doi: 10.1002/jnr.24671. Epub 2020 Jun 18     [PubMed PMID: 32557772]


[3]

Naito H, Hosomi N, Nezu T, Kuzume D, Aoki S, Morimoto Y, Yoshida T, Shiga Y, Kinoshita N, Ueno H, Maruyama H. Prognostic role of the controlling nutritional status score in acute ischemic stroke among stroke subtypes. Journal of the neurological sciences. 2020 Sep 15:416():116984. doi: 10.1016/j.jns.2020.116984. Epub 2020 Jun 12     [PubMed PMID: 32563077]


[4]

Yadav N, Pendharkar H, Kulkarni GB. Spinal Cord Infarction: Clinical and Radiological Features. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. 2018 Oct:27(10):2810-2821. doi: 10.1016/j.jstrokecerebrovasdis.2018.06.008. Epub 2018 Aug 6     [PubMed PMID: 30093205]


[5]

Rouanet C, Reges D, Rocha E, Gagliardi V, Uehara MK, Miranda MA, Silva GS. "Man in the Barrel" Syndrome with Anterior Spinal Artery Infarct due to Vertebral Artery Dissection. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. 2017 Mar:26(3):e41-e42. doi: 10.1016/j.jstrokecerebrovasdis.2016.12.016. Epub 2017 Jan 5     [PubMed PMID: 28065615]


[6]

Segura Bruna N, Munteis Olivas E, Gálvez Ruiz A, Pont Sunyer C, Rodríguez Campello A. [Reversible "man-in-the-barrel" syndrome caused by hypoxic-ischemic encephalopathy]. Neurologia (Barcelona, Spain). 2009 Mar:24(2):133-5     [PubMed PMID: 19322693]


[7]

Torvik A. The pathogenesis of watershed infarcts in the brain. Stroke. 1984 Mar-Apr:15(2):221-3     [PubMed PMID: 6701929]


[8]

Orsini M, Catharino AM, Catharino FM, Mello MP, Freitas MR, Leite MA, Nascimento OJ. Man-in-the-barrel syndrome, a symmetrical proximal brachial amyotrophic diplegia related to motor neuron diseases: a survey of nine cases. Revista da Associacao Medica Brasileira (1992). 2009 Nov-Dec:55(6):712-5     [PubMed PMID: 20191226]

Level 3 (low-level) evidence

[9]

Vainstein G, Gordon CR, Gadoth N. HTLV-1 Associated Motor Neuron Disease Mimicking "Man-in-the-Barrel" Syndrome. Journal of clinical neuromuscular disease. 2005 Mar:6(3):127-31. doi: 10.1097/01.cnd.0000150262.44324.99. Epub     [PubMed PMID: 19078761]


[10]

Irfani Fitri F, Fithrie A, S Rambe A. Association between working memory impairment and activities of daily living in post-stroke patients. Medicinski glasnik : official publication of the Medical Association of Zenica-Doboj Canton, Bosnia and Herzegovina. 2020 Aug 1:17(2):433-438. doi: 10.17392/1135-20. Epub     [PubMed PMID: 32489085]


[11]

Foncea N, Yurrebaso I, Gómez Beldarrain M, García-Moncó JC. [Postoperative bilateral brachial plexopathy mimicking the "man-in-the-barrel" syndrome]. Neurologia (Barcelona, Spain). 2002 Aug-Sep:17(7):388-90     [PubMed PMID: 12236960]


[12]

Díaz-Nicolás S, López-Fernández JC, González-Hernández A, Alemany-Rodríguez MJ, Pérez-Viéitez MC, Araña-Toledo V. [Acute bilateral brachial plexopathy after abdominal surgery mimicking a man-in-the barrel syndrome]. Revista de neurologia. 2008 Dec 16-31:47(12):670-1     [PubMed PMID: 19085889]


[13]

Šaňák D, Divišová P, Hutyra M, Král M, Bártková A, Zapletalová J, Látal J, Dorňák T, Hudec Š, Franc D, Polidar P, Veverka T, Kaňovský P. Risk of recurrent ischemic stroke in young cryptogenic patients with embolic stroke of undetermined source. Journal of the neurological sciences. 2020 Sep 15:416():116985. doi: 10.1016/j.jns.2020.116985. Epub 2020 Jun 13     [PubMed PMID: 32563078]


[14]

Shah PA, Wadia PM. Reversible man-in-the-barrel syndrome in myasthenia gravis. Annals of Indian Academy of Neurology. 2016 Jan-Mar:19(1):99-101. doi: 10.4103/0972-2327.168639. Epub     [PubMed PMID: 27011638]