scholarly journals Resistant hypertension and fetal loss in a patient with fibromuscular dysplasia of the renal artery

2012 ◽  
Vol 18 (2) ◽  
pp. 158-163
Author(s):  
O. O. Bolshakova

We present a clinical case of a young female patient with resistant hypertension and fetal loss. The examination showed a fibromuscular dysplasia of renal artery. Brief literature review of fibromuscular dysplasia is included.

2016 ◽  
Vol 10 ◽  
pp. CMC.S38172
Author(s):  
Paloma Peralta ◽  
Matthew Cholankeril ◽  
Daniel Goldberg ◽  
Jayanth Koneru ◽  
Fayez Shamoon

Renal artery stenosis (RAS) is rare in young patients without fibromuscular dysplasia (FMD). RAS is primarily classified as having two major etiologies, namely, atherosclerosis and FMD, with 90% and 10%, respectively. We report a case of a female in her mid 20s who developed hypertension due to RAS with no evidence of FMD or underlying renal dysfunction and underwent successful angioplasty and stenting.


2019 ◽  
Vol 9 (3) ◽  
pp. 223-228 ◽  
Author(s):  
D. S. Chigidinova ◽  
N. E. Gavrilova ◽  
B. A. Rudenko ◽  
A. S. Shanoyan ◽  
V. P. Mazaev ◽  
...  

Introduction. Fibromuscular dysplasia (FMD) is an idiopathic, non-atherosclerotic, non-inflammatory disease of arteries. Careful research into this disorder showed that FMD has been found in every arterial bed in the body; the most common arteries affected are renal arteries and extracranial sections of carotid and vertebral arteries. The clinical presentation is determined by the localization of the vasculature affected and the stenosis severity. Today FMD is a very rare disease with the incidence of 4 per 1000 people. The diagnosis today is difficult and may take a long time. According to the latest European Society of Cardiology guidelines renal artery balloon angioplasty is indicated for patients with FMD; if a good angiographic result is achieved (no dissection, TIMI 3 flow) no renal artery stenting required. The treatment success depends on the early diagnosis.Materials and Methods. This paper presents a clinical case of renal artery stenosis caused by fibromuscular dysplasia that was treated successfully with balloon angioplasty without stenting.Results and discussion. Protracted process of diagnosing this disease may result in deteriorating quality of life and poor outcomes such as difficult-to-control hypertension and its sequelae, TIA, stroke, aneurism dissection or rupture. It is worth pointing out that FMD diagnosis may be incidental when imaging is performed for other reasons, or when there is a systolic murmur at arteries in an asymptomatic patient who does not have classic atherosclerosis risk factors. According to the latest guidelines endovascular treatment is indicated for patients with FMD to manage the hypertension; this has proven very effective in improving quality of life.


Proceedings ◽  
2019 ◽  
Vol 35 (1) ◽  
pp. 74
Author(s):  
Sorrentino ◽  
Decani ◽  
Zenoni ◽  
Sardella

The aim of this study is to describe a clinical case of a young female patient with oral nevus. [...]


2019 ◽  
Vol 13 (2) ◽  
pp. 119-123
Author(s):  
Yu. I. Khvan ◽  
S. G. Palshina ◽  
V. I. Vasiliev

Cystic and bullous lung transformation occurs in diseases of various origins: neoplastic, genetically determined, rheumatic, lymphoproliferative, and infectious diseases. The paper presents a review of the literature and a clinical case of a young female patient with a long history of Sjögren's disease. Fifteen years after the onset of the disease, the patient developed cystic and bullous lung transformation and renal angiomyolipoma, which are regarded as a manifestation of probable lymphangioleiomyomatosis.


VASA ◽  
2017 ◽  
Vol 46 (4) ◽  
pp. 313-318
Author(s):  
Christina Salmoukas ◽  
Stefan Ruemke ◽  
Jan Hinrich Bräsen ◽  
Axel Haverich ◽  
Omke Enno Teebken

Abstract. Fibromuscular dysplasia is a non-inflammatory, non-atherosclerotic vascular disease, occurring predominantly in younger females. A histologically heterogeneous group of fibroplasia without an inflammatory component causes arterial narrowing. It affects mostly one or both renal arteries, cervicocranial or visceral arteries, leading to hypertension, renal failure/renal infarction or stroke/transient ischaemic attack. We present the case of a young female patient with abdominal aortic coarctation, history of acute renal failure, and critical hypertension due to pseudo-occlusion of both renal arteries. We performed renal artery revascularization specifically by using the Riolan anastomosis as feeding vessel.


Vascular ◽  
2020 ◽  
pp. 170853812097909
Author(s):  
Christian Renz ◽  
Nader Tehrani ◽  
Lillian Malach ◽  
Michael Soult ◽  
Matthew Blecha ◽  
...  

Objective Fibromuscular dysplasia rarely involves vessels other than the renal and carotid arteries. We present a case of a rare fibromuscular dysplasia involving multiple vascular beds in a young female patient with history of spontaneous coronary artery (SCAD). Methods This is a case report with review of the literature using PubMed search for other cases of fibromuscular dysplasia that involves multiple vascular beds and its association with SCAD. The patient agreed to publish her case including her images. Results Fibromuscular dysplasia involving multiple vascular beds in a young female patient with prior coronary dissection is rarely reported in the literature. Conclusion Fibromuscular dysplasia affecting multiple vascular beds is rare but should be suspected in patients with SCAD, particularly young female patients.


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