34 Case report of sertraline exacerbation of tics in tourette’s with OCD

2020 ◽  
Vol 91 (8) ◽  
pp. e22.1-e22
Author(s):  
Mark Paramlall ◽  
Himanshu Tyagi

IntroductionTourette Syndrome (TS) is a prototypical Neuropsychiatric neurodevelopmental disorder consisting of multiple motor tics and at least one vocal tic, usually preceding the motor tic, with onset prior to age 18 and of a duration of at least 1 year.1 2 It is estimated that 50% of TS patients demonstrate OCD behaviours during their lifetime.3 Selective Serotonin Reuptake Inhibitors (SSRI’s) are approved for treatment of depression and for OCD. There are literature reports of the SSRIs, exacerbating or causing tics. However, in all the cases described, symptoms resolved on cessation of Sertraline. We present below a case report of a patient in which this was not the case.Case ReportOur patient was a 22-year-old man an unremarkable medical and psychiatric history except mild childhood tics, resolved in adulthood, was referred with a 3-year history of disabling tics (vocal and motor) of sudden onset after using Sertraline prescribed for depression. Three days post Sertraline he began singing his conversation, swearing and suffering from muscle twitches. His symptoms evolved to include: facial tics (masseter spasms, blinking, puffing of his cheek, expelling air through his lips, forehead wrinkling), complex thoracic and upper limb tics (violent head turnings with a hand grabbing motion, shrugging shoulders with violent right arm movements imitating a severe precordial thump, upper limb shaking with spasms and episodes of punching outwards and upper limb flexion with fingers curled as if he is holding an object such as a gun), Lower limb tics (hip gyration, kicking and occasional foot tapping) and vocal tics (simple and complex). Tics were associated with premonitory urge with increased anxiety and intensity on voluntary inhibition. Investigations were unremarkable and included an LP, blood tests with immunological profile, photo stimulation EEG and an MRI. Unsuccessful treatment modalities employed: CBT for twitches (24 sessions) and psychopharmacological interventions (Risperidone, Haloperidol and Quetiapine. Family history was significant for Sertraline intolerance. He was treated with Aripiprazole 2.5 mg for his diagnosis of Gilles la Tourette syndrome with comorbid OCD.ResultsThe subject responded well to Aripiprazole with reduced tic episodes.ConclusionThe above case is the only one in the literature to identify a family history of sertraline intolerance and requiring treatment with D2 modulator and a 5HT agonist for tic cessation after tic exacerbation post Sertraline treatment.ReferencesRobertson MM, Eapen V. Cavanna AE, et.al. The international prevalence, epidemiology and clinical phenology of Tourette Syndrome: a cross cultural perspective. J Psychosom Res 2009; 67(6): 475–83American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 5th Edition. Arlington (VA): American Psychiatric Association, 2013Leckman JF, Pauls DL, Cohen DJ. Tic disorders. In: Bloom FE, Kupfer DJ. (eds). Psychopharmacology: The fourth Generation of Progress. New York: Raven Press, 1995, 1665–1674

2021 ◽  
pp. 33-38
Author(s):  
João Ribeiro Afonso ◽  
João Carvas ◽  
Miguel Quesado ◽  
João Vasconcelos ◽  
José Vidoedo ◽  
...  

Cystic adventitial disease is a condition where mucinous cyst(s) develop within the adventitia of blood vessels, especially arteries. The most affected vessel is the popliteal artery while the upper limb vasculature is seldom involved. To our knowledge, there are only 2 articles reporting this disease in the ulnar artery. We present a case of a 52-year-old female patient, a manual worker in a clothing factory, with a month history of increasing pain in her right wrist and gradual weakness that incapacitated her for work activities. She was finally treated surgically and an adventitial cyst of the ulnar artery compressing the ulnar nerve was diagnosed.


2005 ◽  
Vol 129 (4) ◽  
pp. 523-526 ◽  
Author(s):  
Shveta Mehra ◽  
Moonja Chung-Park

Abstract We report a case of gallbladder paraganglioma that was discovered during nonrelated surgery. Retrospective study disclosed a family history of pheochromocytoma. The occurrence of gallbladder paraganglioma in the presence of family history of endocrine neoplasia supports that gallbladder paraganglioma may indeed occur as a part of the multiple endocrine neoplasm syndrome. Gallbladder paraganglioma is a rare tumor, and so far to our knowledge only 6 cases have been reported in the literature. Three cases were discovered incidentally during cholecystectomy for cholelithiasis, 2 presented with right upper quadrant pain, and 1 manifested with gastrointestinal bleeding. We herein review all reported cases of paraganglioma of gallbladder and biliary system.


2001 ◽  
Vol 7 (3) ◽  
pp. 559-561
Author(s):  
G. Theodoulou ◽  
G. Milner ◽  
A. Jumaian

1999 ◽  
Vol 8 (6) ◽  
pp. 359-372 ◽  
Author(s):  
Tamsen Caruso Brown ◽  
Judy Garber ◽  
Michael Muto ◽  
Katherine A. Schneider

2005 ◽  
Vol 8 (2) ◽  
pp. 240-244 ◽  
Author(s):  
Chris Wixom ◽  
Amy E. Chadwick ◽  
Henry F. Krous

We report a case of sudden, unexpected death associated with meningioangiomatosis in a 13-year-old, previously healthy male without a history of seizures, neurologic deficits, or clinical stigmata of neurofibromatosis. There was no family history of neurofibromatosis. The postmortem examination showed a 5-cm mass involving the right posterior frontal and orbital frontal cortex that had microscopic features diagnostic of meningioangiomatosis. Because no other cause of death was found, we postulate that he likely died as a result of a seizure secondary to meningioangiomatosis.


Neurosurgery ◽  
1983 ◽  
Vol 13 (6) ◽  
pp. 692-694
Author(s):  
Nancy E. Epstein ◽  
Alan D. Rosenthal ◽  
Jay Selman ◽  
Michael Osipoff ◽  
Roger A. Hyman

Abstract Intracranial gliomas are found in association with von Recklinghausen's neurofibromatosis. However, few truly neonatal lesions have been identified and studied. This case report concerns a 4-month-old child who was found to have a massive thalamic glioma of moderate grade. Four paternal generations had suffered from different manifestations of this transmissible autosomal-dominant (Ad) phakomatosis.


1988 ◽  
Vol 153 (5) ◽  
pp. 689-692 ◽  
Author(s):  
J. C. Powell ◽  
W. R. Silveira ◽  
R. Lindsay

A case of childhood affective disorder with episodes of depressive stupor in a 13-year-old pre-pubertal boy is described. Changes in the patient's clinical state were accompanied by changes in the dexamethasone suppression test. A family history of affective illness on the maternal side, with phenomenological similarities, is noted.


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