Laryngospasm as a single manifestation of epilepsy.
نویسندگان
چکیده
The presence in the hepatic granulomas of eosinophils raised the possibility of Toxocara infestation. Larval remnants were not present within the granulomas nor was there peripheral eosinophilia or any other manifestation of larval migration-for example chorioretinitis. Although there are numerous causes of hepatic granulomas the liver in this case showed features previously reported in extensive Crohn's diseaseO-namely pericholangitis, inflammation of the portal tracts, and increased fibrosis. How should we interpret the presence in our patient of virtual total villus atrophy? Two reports of the coexistance of Crohn's and coeliac diseases are extant7 8; each was associated with other evidence of classical Crohn's disease however, and upon withdrawal of dietary gluten there was clear histological evidence of mucosal recovery. In Crohn's disease per se, a variety of small-bowel mucosal abnormalities has been described.5 These are usually of a patchy nature and are most obvious adjacent to areas of frank mucosal ulceration. The case reported by Daum et al.3 was found initially to have mucosal changes suggestive of coeliac disease on jejunal biopsy but in comparison with our case, the abnormalities were not severe nor did symptoms remit after gluten withdrawal. Our patient requires further study to confirm persisting gluten sensitivity, nevertheless, it seems improbable that the abnormal jejunal histology is a manifestation of Crohn's disease per se.
منابع مشابه
Respiratory Distress as an Isolated Manifestation of Status Epilepticus
Respiratory distress by laryngospasm as an isolated manifestation of epileptic seizure is rare phenomenon. We report on a 1-month-old infant with recurrent respiratory distresses by laryngospasm as an isolated manifestation of status epilepticus and resultant periarrests, while being monitored in our intensive care unit. This case of an atypical manifestation of status epilepticus highlights th...
متن کاملRecurrent meningitis secondary to concealed cerebrospinal fluid otorrhoea.
Laryngospasm as a solitary manifestation of epilepsy is rare. It was reported in a girl who had a long history of repeated seizures.3 Nocturnal dyspnoeic attacks in children were described by Jackson and Jackson4 and defined as 'sudden dyspnoeic seizures' but no electroencephalographic correlates were reported. The usual causes oflaryngospasm, hypocalcaemia, hypoparathyroidism, or hypomagnesaem...
متن کاملSleep-related laryngospasm: a video-polysomnographic recording.
We present a case of laryngospasm in a 12-year-old male who experienced sudden, nocturnal episodes of breathing difficulties and agitation. Apart from laryngospasm, the main differential diagnoses included frontal seizures, sleep-related choking syndrome, sleep asthma, sleep apnoea and REM sleep behaviour disorder. The video and the EEG recordings supported the diagnosis of laryngospasm. The pH...
متن کاملUncommon Manifestation of Complex Partial Seizure in a 7 Years old Child ; a Case Report
Complex partial seizures are known as focal seizures with impaired awareness. Excluding the first year of life, complex partial seizures are the most frequent type of seizures in patients with epilepsy. A detailed history of the patient and family members is a vital element in diagnosing seizures. Although rare, psychotic and anxiety symptoms in individuals may be the result of the seizure. A 7...
متن کاملParoxysmal gaze deviations as the sole manifestation of occipital lobe epilepsy
Paroxysmal gaze deviations as the sole manifestation of occipital lobe epilepsy
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Archives of disease in childhood
دوره 58 2 شماره
صفحات -
تاریخ انتشار 1983