scholarly journals Hirayama disease

2010 ◽  
Vol 01 (01) ◽  
pp. 46-48 ◽  
Author(s):  
Atul T Tayade ◽  
Sushilkumar K Kale ◽  
Arvind Pandey ◽  
Shriprakash Kalantri

ABSTRACTA 17-year-old male, who gave up his favorite sport cricket and started playing football, presented with one-year history of slowly progressive atrophic weakness of forearms and hands. Neurological examination showed weak and wasted arms, forearms and hand but no evidence of pyramidal tract, spinothalmic tract and posterior column lesions. Plain cervical spine radiographs showed no abnormal fi ndings. Cervical magnetic resonance imaging (MRI) showed asymmetric cord atrophy; images obtained with neck fl exed showed the anterior shifting of the posterior wall of the lower cervical dural sac resulting in cord compression. These fi ndings suggest Hirayama disease, a kind of cervical myelopathy related to the fl exion movements of the neck.

2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Minghao Shao ◽  
Jun Yin ◽  
Feizhou Lu ◽  
Chaojun Zheng ◽  
Hongli Wang ◽  
...  

Objective.To evaluate the forward shifting of cervical spinal cords in different segments of patients with Hirayama disease to determine whether the disease is self-limiting.Methods.This study was performed on 11 healthy subjects and 64 patients. According to the duration, the patients were divided into 5 groups (≤1 year, 1-2 years, 2-3 years, 3-4 years, and ≥4 years). Cervical magnetic resonance imaging (MRI) of flexion and conventional position was performed. The distances between the posterior edge of the spinal cord and the cervical spinal canal (X), the anterior and posterior wall of the cervical spinal canal (Y), and the anterior-posterior (A) and the transverse diameter (B) of spinal cord cross sections were measured at different cervical spinal segments (C4 to T1).Results.In cervical flexion position, a significant increase inX/Yof C4-5 segments was found in groups 2–5, the C5-6 and C6-7 segments in groups 1–5, and the C7-T1 segments in group 5 (P<0.05). The degree of the increasedX/Yand cervical flexionX/Yof C5-6 segments were different among the 5 groups (P<0.05), which was likely due to rapid increases inX/Yduring the course of Hirayama’s disease.Conclusion.TheX/Ychange progression indicates that Hirayama disease may not be self-limiting.


2021 ◽  
Vol 14 (10) ◽  
Author(s):  
Farokh Seilanian Toosi ◽  
Malihe Hasanzadeh ◽  
Mona Maftouh ◽  
Ahmadreza Tavassoli

Introduction: Cutaneous metastasis is an uncommon manifestation that mostly occurs in patients with previous gastrointestinal or gynecological malignancies. Local recurrence usually can be seen in surgical incisions. Dysgerminomas are rare ovarian tumors that usually have local invasions, but metastases are infrequent. Here, we described a case of dysgerminoma and cutaneous metastasis in the surgical incision. Case Presentation: The patient was a 39-year-old woman previously known as ovarian dysgerminoma, who had undergone surgery one year ago. Ultrasound examination a year after surgery showed a 35 × 33 millimeters hypoechoic solid tumor in the left ovary and another 3 masses with similar echo pattern and vascularity were found in the surgical incision. Magnetic resonance imaging (MRI) findings were compatible with cutaneous metastasis of pervious dysgerminoma. Pathologic evaluation and Immunohistochemistry (IHC) confirmed dysgerminoma's skin metastasis. She received chemotherapy due to the recurrence of malignancy. Conclusions: Local recurrence and metastases (even in the skin) should be kept in mind and the clinician must examine the surgical site skin in patients with a history of malignancy.


2016 ◽  
Vol 10 (4) ◽  
pp. 370-372 ◽  
Author(s):  
Jivago S. Sabatini ◽  
Gustavo Leopold Schutz-Pereira ◽  
Fabrício Feltrin ◽  
Hélio Afonso Ghizone Teive ◽  
Carlos Henrique Ferreira Camargo

ABSTRACT We present a case report of motor and cognitive disorders in a 36-year-old woman with a history of twelve years of heavy alcohol abuse. The patient presented depressive symptoms over the course of one year after a loss in the family, evolving with ataxia, bradykinesia and choreiform movements. Progressive cognitive decline, sleep alterations and myalgia were also reported during the course of disease evolution. Physical examination revealed spastic paraparesis with fixed flexion of the hips and knees with important pain upon extension of these joints. Initial investigation suggested the diagnosis of thiamine deficiency by brain magnetic resonance imaging (MRI).


2008 ◽  
Vol 56 (3) ◽  
pp. 293-301 ◽  
Author(s):  
Zoe Polizopoulou ◽  
Alexander Koutinas ◽  
Michael Patsikas ◽  
Nektarios Soubasis

The objective of this work was to evaluate the long-term efficacy of a proposed therapeutic protocol in 12 dogs with a tentative diagnosis of degenerative myelopathy, followed-up for a 6-month period. Twelve dogs fulfilling the antemortem inclusion criteria (breed, age, adequate vaccination, history of progressive posterior ataxia and/or paraparesis, no radiographic and myelographic abnormalities in the spinal cord and vertebral column) were allocated. All these dogs presented signs of thoracolumbar syndrome (T3-L3), scored as grade I (mild to moderate ataxia and paraparesis) in 10 and grade II (severe ataxia and ambulatory paraparesis) in 2 cases. Treatment included the use of ɛ-aminocaproic acid and N-acetylcysteine, supplemented with vitamins B, C and E. Prednisolone was given for the first two weeks and upon worsening of neurological signs. Daily exercise, performed as walking or swimming, was strongly recommended. Clinicopathological evaluation was normal in all 12 dogs, and survey radiographs and myelograms did not show spinal cord compression. Magnetic resonance imaging (MRI), performed only in 4 dogs, did not disclose compressive disorders or intramedullary lesions. Neurological signs were progressively worsening in all 12 animals, eventually resulting in severe paraparesis (grade III) or paraplegia (grade IV). The applied medications do not appear to be an attractive alternative to conservative management (physiotherapy) or euthanasia in canine degenerative myelopathy, irrespective of its chronicity.


Author(s):  
Siti Sarah Mohd Ramli ◽  
Asma Abdullah ◽  
Suria Hayati Md Pauzi ◽  
Masturah Ramli

Ceruminous adenoma is described as a glandular neoplasm of ceruminous glands. It is seen for less than one percent of all external ear tumours. Ceruminous adenoma cases were reported to have recurrence and residual tumour, however there was no malignant transformation known in ceruminous adenoma up to this date. Here, we report a young adult woman with two years history of progressive reduced hearing and tinnitus of the right ear. She was proven to have right moderate conductive hearing loss with pure tone audiometry. There was a cystic mass with serous content arising from the posterior wall of the right ear canal. We proceeded with wide local excision of the mass via trans-canal approach. Ceruminous adenoma was confirmed with histopathology and immunohistochemistry of CK7 staining. The hearing impairment was resolved completely post excision and there was no recurrence of the tumour on one year follow-up. We concluded wide local excision with appropriate margin of the mass is adequate to prevent recurrence in ceruminous adenoma cases.


Author(s):  
Ejaz Ahmed Sheriff ◽  
Swaminathan Vaidyanathan ◽  
Dinesh Kumar Chandran ◽  
Kumar Chidambaram ◽  
Latchumanadhas Kalidas ◽  
...  

Study report a 42-years-old female came with complaints of dyspnoea on exertion, and recurrent cough for past one year. She gives history of significant weight loss for the past 6 months. Trans thoracic echocardiogram showed large pedunculated myxoma measuring 28*18 mm attached to posterior wall of right atrium extending into right ventricle and outflow tract. Computed tomography pulmonary angiogram showed acute bilateral pulmonary thromboembolism with left upper lobe infarct. She underwent complete removal of the tumour along with patch of atrial wall with pulmonary embolectomy using Fogarty baloon catheter through median sternotomy. Her postoperative course was uneventful. This case is reported for its rarity of presentation of right atrial myxoma with pulmonary embolism.


Neurology ◽  
2021 ◽  
pp. 10.1212/WNL.0000000000012580
Author(s):  
Nathan W Churchill ◽  
Michael G Hutchison ◽  
Simon J Graham ◽  
Tom A Schweizer

Objective:To test the hypothesis that a history of concussion (HOC) causes greater disturbances in cerebral blood flow (CBF) and white matter microstructure of midline brain structures after subsequent concussions, during the acute and chronic phases of recovery.Methods:In this longitudinal magnetic resonance imaging (MRI) study, 61 athletes with uncomplicated concussion (36 with HOC) were imaged at the acute phase of injury (1 to 7 days post-injury), the subacute phase (8 to 14 days), medical clearance to return to play (RTP), one month post-RTP and one year post-RTP. A normative group of 167 controls (73 with HOC) were also imaged. Each session assessed CBF of the cingulate cortex, along with fractional anisotropy (FA) and mean diffusivity (MD) of the corpus callosum. Linear mixed models tested for interactions of HOC with time post-injury. The sport concussion assessment tool (SCAT) was also used to evaluate effects of HOC on symptoms, cognition and balance.Results:Athletes with HOC had greater declines in midcingulate CBF subacutely (z=-3.29, p=0.002) and greater declines in posterior cingulate CBF at one year post-RTP (z=-2.42, p=0.007). No significant effects of HOC were seen for FA, whereas athletes with HOC had higher MD of the splenium at RTP (z=2.54, p=0.008). These effects were seen in the absence of differences in SCAT domains (|z|<1.14, p>0.256) or time to RTP (z=0.23, p=0.818).Conclusions:Results indicate subacute and chronic effects of HOC on cingulate CBF and callosal microstructure, in the absence of differences in clinical indices. These findings provide new insights into physiological brain recovery after concussion, with cumulative effects of repeated injury detected among young, healthy athletes.


2014 ◽  
Vol 20 (2) ◽  
pp. 191-195 ◽  
Author(s):  
Igor Paredes ◽  
Jesus Esteban ◽  
Ana Ramos ◽  
Pedro Gonzalez ◽  
Juan José Rivas

Hirayama disease, or juvenile amyotrophy of distal upper extremity, is a benign, self-limiting cervical myelopathy consisting of selective unilateral weakness of the hand and forearm. The weakness slowly progresses until spontaneous arrest occurs within 5 years of onset. The condition predominantly affects Asian males and is thought to be secondary to spinal cord compression during neck flexion, because of a forward displacement of the posterior dural sac. The authors present what is to their knowledge the first reported case of a Caucasian male with a severe form of Hirayama disease, suffering from weakness of the leg as well as the forearm. An abnormal range of cervical flexion was observed at the C5–6 level. The patient was successfully treated by anterior cervical discectomy and fusion.


1970 ◽  
Vol 18 (1) ◽  
pp. 51-52
Author(s):  
Md L Rahman ◽  
ASM Shawkat Ali ◽  
MI Alam

A 45-year-old female presented with weakness of lower extremities with history of simple mastectomy one year back. On myelographic examination showed complete block at mid thoracic level which is extra-dural in nature. On operation extra-dural large mass compressing the spinal cord at T5 level was detected.   doi: 10.3329/taj.v18i1.3306 TAJ 2005; 18(1): 51-52


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