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Intermittent bursts of abdominal wall jerky movements: belly dancers syndrome? Osama S M Amin, 1 Qalandaar Hussein Abdulkarim, 2 Mohammad Shaikhani 3 1 Department of Neurology, Sulaimaniya General Teaching Hospital, Sulaimaniya City, Iraq 2 Department of Surgery, Sulaimaniya General Teaching Hospital, Sulaimaniya City, Iraq 3 Department of Internal Medicine, Sulaimaniya General Teaching Hospital, Sulaimaniya City, Iraq Correspondence to Dr Osama S M Amin, [email protected] To cite: Amin OSM, Abdulkarim QH, Shaikhani M. BMJ Case Reports Published online: 24 December 2012 doi:10.1136/bcr-2012- 007393 DESCRIPTION A 47-year-old Iraqi Kurdish woman presented with a 1-day history of sudden onset of frequent, inter- mittent and painful abdominal wall jerky move- ments, 6 days after undergoing haemorrhoidectmy. During sleep, these movements were absent. The postoperative period was uneventful and the patient was discharged home on day 2 with oral clindamycine and metronidazole. The appearance of these movements prompted the A&E interns to think about intestinal obstruction and accordingly they consulted the general surgical department; the surgeon suggested symptomatic treatment with watchful waiting and nothing by mouth. However, on day 3, we were asked to examine the patient; these movements (video 1) represented belly dancers syndrome. Brain and spinal MRI were unremarkable, as were her blood tests, chest CT scan and transthoracic echocardiography; diaphrag- matic uoroscopy and abdominal wall/diaphrag- matic electromyography were not done. She was prescribed intravenous diphenhydramine and oral diazepam; her complaints disappeared completely 3 days later and have never recurred. Belly dancers syndrome (or diaphragmatic utter) refers to myoclonic jerks involving one or both hemidiaphragms, which are involuntary, repeti- tive, usually painful and often rhythmic, and result in visible undulating movements of the abdomen (and sometimes the trunk), an appearance which resembles belly dance. The condition is rare and has a long list of causes. The core feature is a rapid myo- clonic contraction and release of the diaphragm, which, in most cases, involves both inspiration and expiration. The majority is bilateral, but unilateral cases usually target the left side. The abdomen is usually painful and the dyspnoea is frequently a prominent complaint. 13 Learning points Belly dancers syndrome is a form of diaphragmatic myoclonic jerks (or utter) which can result in chest and/or abdominal pain and dyspnoea. Therefore, an alternative diagnosis usually comes to mind. Clinically, frequent, intermittent and often rhythmic involuntary undulations of the abdomen are observed. Diaphragmatic uoroscopy and electromyography are the key diagnostic tools. In spite of the long list of pathologically dened causes behind this syndrome, several cases are idiopathic and some are psychogenic. Competing interests None. Patient consent Obtained. Provenance and peer review Not commissioned; externally peer reviewed. REFERENCES 1 Rigatto M, De Medeiros NP. Diaphragmatic utter: report of a case and review of the literature. Am J Med 1962;32:1039. 2 Kobayashi I, Tazaki G, Hayama N, et al. A case of the diaphragmatic utter with an electromyographic study of the respiratory muscles. Tokai J Exp Clin Med 2004;29:1514. 3 Linazasoro G, Blercom N, Lasa A, et al. Etiological and therapeutical observations in a case of belly dancers dyskinesia. Mov Disord 2005;20:2513. Video 1 Note the undulating movements of the anterior abdominal wall muscles, which are more prominent on the left side and resemble belly dancing. This is the diaphragmatic utter of belly dancers syndrome and is a form of myoclonic jerks. Amin OSM, et al. BMJ Case Reports 2012. doi:10.1136/bcr-2012-007393 1 Images in on 7 April 2020 by guest. Protected by copyright. http://casereports.bmj.com/ BMJ Case Reports: first published as 10.1136/bcr-2012-007393 on 24 December 2012. Downloaded from

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Intermittent bursts of abdominal wall jerkymovements belly dancerrsquos syndromeOsama S M Amin1 Qalandaar Hussein Abdulkarim2 Mohammad Shaikhani3

1Department of NeurologySulaimaniya General TeachingHospital Sulaimaniya City Iraq2Department of SurgerySulaimaniya General TeachingHospital Sulaimaniya City Iraq3Department of InternalMedicine Sulaimaniya GeneralTeaching Hospital SulaimaniyaCity Iraq

Correspondence toDr Osama S M Amindrosamaamingmailcom

To cite Amin OSMAbdulkarim QHShaikhani M BMJ CaseReports Published online 24December 2012doi101136bcr-2012-007393

DESCRIPTIONA 47-year-old Iraqi Kurdish woman presented witha 1-day history of sudden onset of frequent inter-mittent and painful abdominal wall jerky move-ments 6 days after undergoing haemorrhoidectmyDuring sleep these movements were absent Thepostoperative period was uneventful and thepatient was discharged home on day 2 with oralclindamycine and metronidazole The appearanceof these movements prompted the AampE interns tothink about intestinal obstruction and accordinglythey consulted the general surgical department thesurgeon suggested symptomatic treatment withwatchful waiting and nothing by mouth Howeveron day 3 we were asked to examine the patientthese movements (video 1) represented bellydancerrsquos syndrome Brain and spinal MRI wereunremarkable as were her blood tests chest CTscan and transthoracic echocardiography diaphrag-matic fluoroscopy and abdominal walldiaphrag-matic electromyography were not done She wasprescribed intravenous diphenhydramine and oraldiazepam her complaints disappeared completely3 days later and have never recurred

Belly dancerrsquos syndrome (or diaphragmaticflutter) refers to myoclonic jerks involving one orboth hemidiaphragms which are involuntary repeti-tive usually painful and often rhythmic and resultin visible undulating movements of the abdomen(and sometimes the trunk) an appearance whichresembles belly dance The condition is rare and hasa long list of causes The core feature is a rapid myo-clonic contraction and release of the diaphragmwhich in most cases involves both inspiration andexpiration The majority is bilateral but unilateralcases usually target the left side The abdomen isusually painful and the dyspnoea is frequently aprominent complaint1ndash3

Learning points

Belly dancerrsquos syndrome is a form ofdiaphragmatic myoclonic jerks (or flutter)which can result in chest andor abdominalpain and dyspnoea Therefore an alternativediagnosis usually comes to mind

Clinically frequent intermittent and oftenrhythmic involuntary undulations of theabdomen are observed

Diaphragmatic fluoroscopy andelectromyography are the key diagnostic toolsIn spite of the long list of pathologicallydefined causes behind this syndrome severalcases are idiopathic and some are psychogenic

Competing interests None

Patient consent Obtained

Provenance and peer review Not commissioned externally peerreviewed

REFERENCES1 Rigatto M De Medeiros NP Diaphragmatic flutter report of a case

and review of the literature Am J Med 196232103ndash92 Kobayashi I Tazaki G Hayama N et al A case of the

diaphragmatic flutter with an electromyographic study of therespiratory muscles Tokai J Exp Clin Med 200429151ndash4

3 Linazasoro G Blercom N Lasa A et al Etiological andtherapeutical observations in a case of belly dancerrsquos dyskinesiaMov Disord 200520251ndash3

Video 1 Note the undulating movements of theanterior abdominal wall muscles which are moreprominent on the left side and resemble belly dancingThis is the diaphragmatic flutter of belly dancerrsquossyndrome and is a form of myoclonic jerks

Amin OSM et al BMJ Case Reports 2012 doi101136bcr-2012-007393 1

Images inhellip

on 7 April 2020 by guest P

rotected by copyrighthttpcasereportsbm

jcom

BM

J Case R

eports first published as 101136bcr-2012-007393 on 24 Decem

ber 2012 Dow

nloaded from

Copyright 2012 BMJ Publishing Group All rights reserved For permission to reuse any of this content visithttpgroupbmjcomgrouprights-licensingpermissionsBMJ Case Report Fellows may re-use this article for personal use and teaching without any further permission

Become a Fellow of BMJ Case Reports today and you can Submit as many cases as you like Enjoy fast sympathetic peer review and rapid publication of accepted articles Access all the published articles Re-use any of the published material for personal use and teaching without further permission

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2 Amin OSM et al BMJ Case Reports 2012 doi101136bcr-2012-007393

Images inhellip

on 7 April 2020 by guest P

rotected by copyrighthttpcasereportsbm

jcom

BM

J Case R

eports first published as 101136bcr-2012-007393 on 24 Decem

ber 2012 Dow

nloaded from

Copyright 2012 BMJ Publishing Group All rights reserved For permission to reuse any of this content visithttpgroupbmjcomgrouprights-licensingpermissionsBMJ Case Report Fellows may re-use this article for personal use and teaching without any further permission

Become a Fellow of BMJ Case Reports today and you can Submit as many cases as you like Enjoy fast sympathetic peer review and rapid publication of accepted articles Access all the published articles Re-use any of the published material for personal use and teaching without further permission

For information on Institutional Fellowships contact consortiasalesbmjgroupcom

Visit casereportsbmjcom for more articles like this and to become a Fellow

2 Amin OSM et al BMJ Case Reports 2012 doi101136bcr-2012-007393

Images inhellip

on 7 April 2020 by guest P

rotected by copyrighthttpcasereportsbm

jcom

BM

J Case R

eports first published as 101136bcr-2012-007393 on 24 Decem

ber 2012 Dow

nloaded from