Abdominal epilepsia partialis continua due to cortical ischemia: a video-documented case report and review

2020 ◽  
Author(s):  
Morgane Soler-Rico ◽  
Roger Denays ◽  
Eléonore Sinzobahamvya
Keyword(s):  
Case Report ◽  
Epilepsia Partialis Continua ◽  
Documented Case ◽  
Cortical Ischemia

Benefit of vagal nerve stimulation in epilepsia partialis continua: a case report

2006 ◽  
Vol 37 (03) ◽  
Author(s):  
C Bussmann ◽  
HM Meinck ◽  
HH Steiner ◽  
W Broxtermann ◽  
CG Bien ◽  
...  
Keyword(s):  
Case Report ◽  
Nerve Stimulation ◽  
Vagal Nerve ◽  
Vagal Nerve Stimulation ◽  
Epilepsia Partialis Continua

Primary squamous carcinoma of the thyroid–a case report

1993 ◽  
Vol 107 (12) ◽  
pp. 1155-1158 ◽  
Author(s):  
Claes Theander ◽  
Brita Lödén ◽  
Jan Berglund ◽  
Tomas Seidal
Keyword(s):  
Thyroid Cancer ◽  
Case Report ◽  
Primary Tumour ◽  
Squamous Carcinoma ◽  
Documented Case

We report a well-documented case of fatal thyroid cancer with histopathological characteristics of primary squamous carcinoma. A possible primary tumour elsewhere was excluded. The possible histogenesis of this unusual tumour and the therapy of choice are briefly discussed.

scholarly journals Epilepsia partialis continua present with shoulder joint-trunk-hip joint rhythmic clonic seizure: a case report

2016 ◽  
Vol Volume 12 ◽  
pp. 2363-2366 ◽  
Author(s):  
Yudan Lv ◽  
Wang Zan ◽  
Fengna Chu ◽  
Chang Liu ◽  
Hongmei Meng
Keyword(s):  
Case Report ◽  
Hip Joint ◽  
Shoulder Joint ◽  
Clonic Seizure ◽  
Epilepsia Partialis Continua

scholarly journals FIRST REPORT ON OTOTOXICITY OF MEGLUMINE ANTIMONIATE

2014 ◽  
Vol 56 (5) ◽  
pp. 439-442 ◽  
Author(s):  
Cláudia Maria Valete-Rosalino ◽  
Maria Helena Araujo-Melo ◽  
Débora Cristina de Oliveira Bezerra ◽  
Renata Oliveira de Barcelos ◽  
Vanessa de Melo-Ferreira ◽  
...  
Keyword(s):  
Case Report ◽  
Auditory Threshold ◽  
First Report ◽  
Meglumine Antimoniate ◽  
Documented Case ◽  
Drug Of Choice ◽  
Tegumentary Leishmaniasis ◽  
Vestibular Toxicity

Introduction: Pentavalent antimonials are the first drug of choice in the treatment of tegumentary leishmaniasis. Data on ototoxicity related with such drugs is scarcely available in literature, leading us to develop a study on cochleovestibular functions. Case Report: A case of a tegumentary leishmaniasis patient, a 78-year-old man who presented a substantial increase in auditory threshold with tinnitus and severe rotatory dizziness during the treatment with meglumine antimoniate, is reported. These symptoms worsened in two weeks after treatment was interrupted. Conclusion: Dizziness and tinnitus had already been related to meglumine antimoniate. However, this is the first well documented case of cochlear-vestibular toxicity related to meglumine antimoniate.

scholarly journals Epilepsia partialis continua complicated by disseminated tuberculosis and hemophagocytic lymphohistiocytosis: a case report

2019 ◽  
Vol 13 (1) ◽  
Author(s):  
Gashirai K. Mbizvo ◽  
Isabel C. Lentell ◽  
Clifford Leen ◽  
Huw Roddie ◽  
Christopher P. Derry ◽  
...  
Keyword(s):  
Case Report ◽  
Hemophagocytic Lymphohistiocytosis ◽  
Epilepsia Partialis Continua ◽  
Disseminated Tuberculosis

Heparin-Induced Fever: A Case Report and Literature Review

2019 ◽  
Vol 40 (5) ◽  
pp. 723-724 ◽  
Author(s):  
Jake Laun ◽  
Katie Laun ◽  
Adeel Farooqi ◽  
David J Smith
Keyword(s):  
Case Report ◽  
Systemic Inflammatory Response Syndrome ◽  
Literature Review ◽  
Inflammatory Response ◽  
Systemic Inflammatory Response ◽  
Burn Patients ◽  
Drug Induced ◽  
Documented Case

Abstract Burn patients are often plagued by fever due to the inflammatory nature of their injuries as well as the normal postoperative systemic inflammatory response syndrome. One etiology for fever, often not initially considered, is drug-induced fever. A rare cause of drug-induced fever is heparin with only one documented case reported in the literature. We present a case of heparin-induced fever in a patient who experienced a 32% total BSA friction burn after a motorcycle crash.

Schizophrenia and Klinefelter's Syndrome

1981 ◽  
Vol 26 (4) ◽  
pp. 262-264 ◽  
Author(s):  
Alec Roy
Keyword(s):  
Case Report ◽  
Psychiatric Disorder ◽  
Klinefelter’S Syndrome ◽  
Klinefelter's Syndrome ◽  
Documented Case

Psychiatric disorder in relation to Klinefelter's syndrome is reviewed. A well documented case report is presented of a schizophreniform illness in a patient with Klinefelter's.

scholarly journals Intracranial Capillary Hemangioma in the Posterior Fossa of an Adult Male

2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Jordan Nepute ◽  
Jinping Lai ◽  
Yihua Zhou
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Posterior Fossa ◽  
Adult Male ◽  
Capillary Hemangioma ◽  
Rare Entity ◽  
Documented Case ◽  
Imaging Appearance

Intracranial capillary hemangioma (ICH) is a rare entity, with approximately 24 reported cases in the literature. There are only three reported cases of ICH in an adult male. In this case report, we describe the fourth documented case of ICH in an adult male and, to the best of our knowledge, the first ever documented case of ICH in the posterior fossa of an adult male. We also discuss its imaging appearance and differential diagnosis.

Lupus nephritis in a Nigerian child: A first documented case report in South-East Nigeria

2013 ◽  
Vol 6 (3) ◽  
pp. 335
Author(s):  
OdetundeO Israel ◽  
EzeonwuB Uzoma ◽  
OkaforH Uche ◽  
UwaezuokeS Nkachukwu ◽  
AdieleK Daberchi ◽  
...  
Keyword(s):  
Case Report ◽  
Lupus Nephritis ◽  
Documented Case ◽  
Nigerian Child

scholarly journals Poland’s syndrome: a rare case report

2017 ◽  
Vol 4 (10) ◽  
pp. 3526 ◽  
Author(s):  
Reshma S. ◽  
Vijai R. ◽  
Chakarvarthy N.
Keyword(s):  
Case Report ◽  
Chest Wall ◽  
Male Patient ◽  
Rare Case ◽  
Pectoralis Major Muscle ◽  
Poland’S Syndrome ◽  
Documented Case ◽  
Poland's Syndrome ◽  
Rare Case Report ◽  
Congenital Condition

Poland’s syndrome is a rare congenital condition. It is classically characterized by absence of unilateral chest wall muscles and sometimes ipsilateral symbrachydactyly (abnormally short and webbed fingers). The condition typically presents with unilateral absence of the sternal or breast bone portion of the pectoralis major muscle which may or may not be associated with the absence of nearby musculoskeletal structures. We report a 25-year-old male patient with typical features of Poland’s syndrome. To the best of our knowledge, this is the first documented case of a patient with Poland’s syndrome reported from Chennai.

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