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Mycobacterium tuberculosis in the aorta of a patient with takayasu’s arteritis. extra pulmonary tuberculosis

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Health 2011年第3期3卷 159-161页

作者： María Elena Soto Virgilia Soto Julia Isela Martín Sandría Ricardo Gamboa Claudia Huesca 不详

Takayasu’s arteritis (TA), of unknown etiology, has been related with Mycobacterium tuberculosis infection. The published cases are controversial. A 29- year-old man died, prolapse of the aortic valve and unspecific arteritis were demonstrated at necropsy. Our objective was to search in the fresh aortic tissues, the infectious agent of tuberculosis through culture, as well as by performing histopathology and searching by the molecular study, sequences of genes associated to micobacteria and Ziehl’s stain. Results. The bacillus of tuberculosis was observed by the Ziehl’s stain and the sequences of insertion IS6110 gene were identified. Our findings support the relation of TA with possible tuberculosis infection.Conclusion. The possibility that Takayasu’s arteritis is an extra pulmonary tu-berculosis must be explored.

关键词： Takayasu’s arteritis extrapulmonary tuberculosis IS6110 and HupB sequences

Takayasu’s arteritis-aphasia as an initial presentation

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Neuroimmunology and Neuroinflammation 2016年第1期3卷 192-195页

作者： Davinder Singh Rana Anuradha Batra Ish Anand Samir Patel Pooja Gupta Department of Neurology Old building blockSir Ganga Ram HospitalOld Rajinder NagarNew Delhi 110060India

Takayasu arteritis(TA)is an uncommon disease of young women,characterized by granulomatous vasculitis of medium and large arteries.Neurological involvement is reported in only a minority of patients and occurrence of neurological syndromes as the first manifestation of disease has been rarely reported.We present clinical,laboratory and imaging findings of a 40 years old lady with TA,who initially presented with clinical manifestations of stroke in form of aphasia.The rarity of the disease and especially such a presentation can cause considerable delay in the diagnosis and treatment.

关键词： Takayasu arteritis stroke aphasia

Erdheim-Chester Disease with Right Atrial Tumor and “Temporal arteritis”

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Open Journal of Rheumatology and Autoimmune Diseases 2012年第3期2卷 37-38页

作者： Joseph Skalski William D. Edwards Eric L. Matteson Department of Internal Medicine Mayo Clinic College of Medicine Rochester Minnesota USA Department of Pathology Mayo Clinic College of Medicine Rochester USA Division of Rheumatology Mayo Clinic College of Medicine Rochester USA

Erdheim-Chester disease is an unusual syndrome characterized by non-Langerhans cell histiocytosis which can mimic rheumatologic diseases. We report a case of Erdheim-Chester masquerading as giant cell arteritis, which... 详细信息

关键词： Erdheim-Chester Disease Temporal arteritis Giant Cell arteritis

Prevalence and long-term prognosis in Takayasu arteritis patients with left ventricular dilatation and a decreased ejection fraction:data from 1,105 Chinese cases

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中国循环杂志 2018年第S1期33卷 143-143页

作者： Ying Zhang Peng Fan Fang Luo Xianliang Zhou National Center for Cardiovascular Diseases Fuwai HospitalChinese Academy of Medical Sciences and Peking Union Medical CollegeBeijingChina

Background Left ventricular dilatation and a decreased ejection fraction is one of the most serious complications in patients with Takayasu arteritis(TA).We aim to describe the prevalence,clinical features,treatment,a... 详细信息

关键词： Takayasu arteritis left ventricular dilatation Prevalence long-term prognosis

Malignancy in Chinese patients with Takayasu arteritis

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中国循环杂志 2018年第S1期33卷 145-145页

作者： Ying Zhang Fang Luo Xianliang Zhou Department of Cardiology National Center for Cardiovascular DiseasesFuwai HospitalChinese Academy of Medical Sciences and Peking Union Medical CollegeBeijingChina

Objective Takayasu arteritis(TA)is a kind of large vessel vasculitis of unknown reason.Autoimmune disorder was perhaps one of the risk factors.Cancer was related to autoimmune disease.This study aimed to describe the ... 详细信息

关键词： Takayasu arteritis risk factors autoimmune disease

Takayasu Disease in Niger: About Three Cases and Literature Review

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Open Journal of Internal Medicine 2019年第4期9卷 129-140页

作者： E. Adehossi B. M. Charfo S. Brah M. Daou A. Andia A. Salia D. I. Bako H. Bako H. Idrissa R. Sani Department of Internal Medicine Hôpital National de Niamey Niamey Niger Department of Radiology Hôpital National de Niamey Niamey Niger Department of Cardiology Hôpital National de Niamey Niamey Niger Department of General Surgery Hôpital National de Niamey Niamey Niger

Takayasu arteritis is a chronic, idiopathic, and inflammatory disease that primarily affects large vessels, such as the aorta and its main branches. Much of the literature describing Takayasu arteritis has originated from Asian countries, and the disease was once thought to be restricted to these regions. During the past few decades, patients with Takayasu arteritis have been increasingly recognized in Africa. We report three first cases of Takayasu’s arteritis in Niger by focusing on epidemiological clinical radiological and therapeutic aspects. Of the three patients, two were women and the age of onset was 27 years in one case and 33 years in the other two cases. Clinically, abolition of at least one peripheral pulse was constantly observed. We find a predominance of the involvement of the supra-aortic trunks in 3 cases and less of the abdominal aortic involvement in 1 case. Moreover, our series is distinguished by a case revealed by a stroke in a male subject. Corticosteroids were successful with clinical improvement and stabilization of the disease in the short and medium term. The revascularization performed in two of the patients. Tayasu arteritis is uncommon disease that must be evoked before a symptomatology non-specific coaches and lead to check the pulse. Ischemic complications are already present at the time of diagnosis. We have found a high frequency of arterial thrombosis in our series.

关键词： Takayasu arteritis Niamey Niger

CARDIOVASCULAR SYSTEM

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China Medical Abstracts(Internal Medicine) 1996年第1期13卷 20-25页

Cardiovascular System

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China Medical Abstracts(Internal Medicine) 2012年第2期29卷 89-95页

Retinal hemorrhage as a unique ophthalmic manifestation of cerebral hyper perfusion syndrome

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World Journal of Cardiovascular Diseases 2013年第3期3卷 336-338页

作者： Eitan Heldenberg Arie Bass Department of Vascular Surgery Assaf Harofeh Medical Center Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel

Cerebral hyperperfusion syndrome (CHPS) is a rare, complication of carotid artery revascularization. Acute retinal hemorrhage is a very rare entity previously described as a manifestation of CHPS following carotid artery stenting (CAS), but to the best of our knowledge, not yet described as a complication of carotid surgery. An Ascending Aorta to bilateral Carotid bypass was performed in a 35-year-old woman with active Takayasu arteritis and 95% symptomatic stenosis of both common carotid arteries. Severe retinal hemorrhage appeared on the second post operative day combined with high blood pressure, brain edema on CT scan and grand mal seizures. It seems that fundoscopic examination following carotid revascularization of tight can be helpful in identifying those patients who develop symptoms suggesting of CHPS.

关键词： Cerebral Hyper Perfusion Syndrome Takayasu arteritis Retinal Hemorrhage