A rare case of fibromuscular dysplasia involving multiple vascular beds

Vascular ◽  
2020 ◽  
pp. 170853812097909
Author(s):  
Christian Renz ◽  
Nader Tehrani ◽  
Lillian Malach ◽  
Michael Soult ◽  
Matthew Blecha ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Case ◽  
Carotid Arteries ◽  
Fibromuscular Dysplasia ◽  
Young Female ◽  
Review Of The Literature ◽  
Pubmed Search ◽  
History Of ◽  
Vascular Beds

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.

Development of lymphangioleiomyomatosis in a female patient with Sjö gren's disease: a review of literature and a case report

2019 ◽  
Vol 13 (2) ◽  
pp. 119-123
Author(s):  
Yu. I. Khvan ◽  
S. G. Palshina ◽  
V. I. Vasiliev
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Clinical Case ◽  
Young Female ◽  
Renal Angiomyolipoma ◽  
Review Of Literature ◽  
Review Of The Literature ◽  
History Of ◽  
Genetically Determined ◽  
Sjögren’S Disease

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.

scholarly journals A rare case of eight multiple primary malignant neoplasms in a female patient: A case report and review of the literature

2014 ◽  
Vol 9 (2) ◽  
pp. 587-590 ◽  
Author(s):  
JIEMIN ZHAO ◽  
YAN TAN ◽  
YUGANG WU ◽  
WEI ZHAO ◽  
JUN WU ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Case ◽  
Malignant Neoplasms ◽  
Review Of The Literature ◽  
Multiple Primary

scholarly journals Laparoscopic resection of a sigmoid colon lipoma in a young female patient: A case report and review of the literature

2017 ◽  
Vol 13 (3) ◽  
pp. 1303-1306 ◽  
Author(s):  
Georgios I. Panagiotakis ◽  
Alexandros G. Andreou ◽  
Ioannis E. Petrakis ◽  
Maria Tzardi ◽  
Maria Daskalogiannaki ◽  
...  
Keyword(s):  
Case Report ◽  
Sigmoid Colon ◽  
Female Patient ◽  
Laparoscopic Resection ◽  
Young Female ◽  
Review Of The Literature

scholarly journals Stridor and respiratory failure due to tracheobronchomalacia: case report and review of the literature

2012 ◽  
Vol 130 (1) ◽  
pp. 61-64 ◽  
Author(s):  
Ramon Andrade de Mello ◽  
Adriana Magalhães ◽  
Abílio José Vilas-Boas
Keyword(s):  
Case Report ◽  
Respiratory Failure ◽  
Rare Case ◽  
Rigid Bronchoscopy ◽  
Chronic Obstructive ◽  
Review Of The Literature ◽  
Cross Sectional ◽  
Obstructive Pulmonary Disease ◽  
Copd Patients ◽  
History Of

CONTEXT: Tracheobronchomalacia (TBM) results from structural and functional abnormalities of the respiratory system. It is characterized by excessive collapse: at least 50% of the cross-sectional area of the trachea and main bronchi. In this paper, we present a rare case of a patient with TBM who first presented with stridor and respiratory failure due to exacerbation of chronic bronchitis. CASE REPORT: An 81-year-old Caucasian man was admitted presenting coughing, purulent sputum, stridor and respiratory failure. He had a medical history of chronic obstructive pulmonary disease (COPD) and silicosis and was a former smoker. Axial computed tomography on the chest revealed marked collapse of the trachea in its middle third. Bronchoscopy showed characteristics compatible with TBM. He was treated with noninvasive ventilation, without any good response. Subsequently, a Dumon Y stent was placed by means of rigid bronchoscopy. After the procedure, he was discharged with a clinical improvement. CONCLUSION: TBM is fatal and often underdiagnosed. In COPD patients, stridor and respiratory failure may be helpful signs that should alert physicians to consider TBM as an early diagnosis. Thus, these signs may be important for optimizing the treatment and evolution of such patients.

scholarly journals Renal Metastases of a Femur Osteosarcoma: A Case Report and a Review of the Literature

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Yousra Akasbi ◽  
Samia Arifi ◽  
Karim Lahlaidi ◽  
Tarik Namad ◽  
Nawfel Mellas ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
English Literature ◽  
Renal Involvement ◽  
Review Of The Literature ◽  
Metastatic Osteosarcoma ◽  
History Of ◽  
Renal Metastases

This paper discusses a rare case of renal metastatic osteosarcoma. A 25-year-old man with a history of metastatic osteosarcoma involving his right kidney was referred to our institution for treatment. He was managed with chemotherapy. An exhaustive review of the English literature pertaining to this disease was performed. To our knowledge, this case represents only the sixteenth. The literature suggests that the incidence of renal involvement in osteosarcoma is significant and that the treatment should be multidisciplinary in such patients.

scholarly journals Metastasis of Colorectal Adenocarcinoma to the Thyroid: A Case Report and Review of the Literature

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
C. Goatman ◽  
P. J. Goldsmith ◽  
V. Antonopoulos ◽  
B. Ali
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Colorectal Adenocarcinoma ◽  
Review Of The Literature ◽  
Thyroid Lesion ◽  
Acute Presentation ◽  
History Of ◽  
Thyroid Metastases ◽  
Colorectal Tumours ◽  
Metastasis To The Thyroid

Purpose. We present a rare case of colorectal metastasis to the thyroid five years following primary colonic resection. This case highlights the need to be cognisant of unusual sites of metastasis from colorectal neoplasms.Case Report. An 82-year-old male patient had a panproctocolectomy for synchronous colorectal tumours. Five years later he was found to have lung and thyroid metastases found incidentally on imaging for an acute presentation with small bowel obstruction.Conclusion. Metastases to the thyroid should be considered in the differential diagnosis of the thyroid lesion with any history of malignancy, particularly with increasing patient age and when renal cell carcinoma or lung, colon, or breast primaries are involved.

scholarly journals A rare giant gastric trichobezoar in a young female patient: Case report and review of the literature

2021 ◽  
Vol 9 (12) ◽  
Author(s):  
Dimitra G. Delimpaltadaki ◽  
Ioannis G. Gkionis ◽  
Mathaios E. Flamourakis ◽  
Andreas F. Strehle ◽  
Emmanouil N. Bachlitzanakis ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Young Female ◽  
Review Of The Literature ◽  
Patient Case ◽  
Gastric Trichobezoar

Cystic Falcine Chondroma: Case Report and Review of the Literature

Neurosurgery ◽  
1991 ◽  
Vol 29 (6) ◽  
pp. 909-912 ◽  
Author(s):  
Karim Hadadian ◽  
Hossein Abtahii ◽  
Zahra T. Asil ◽  
Mohammad Rakhshan ◽  
Parvin Vessal
Keyword(s):  
Case Report ◽  
Microscopic Examination ◽  
Rare Case ◽  
Cystic Degeneration ◽  
Review Of The Literature ◽  
Resected Tumor ◽  
History Of

Abstract A rare case of falcine chondroma in a 25-year-old woman with an 8-year history of headache and a recent generalized seizure is presented. Microscopic examination of the resected tumor revealed that it was a falcine chondroma with chondrocytes and central cystic degeneration.

scholarly journals Gastric Medullary Carcinoma: A Rare Case Report

2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Ferit Aslan ◽  
Fisun Ardıç Yükrük ◽  
Fatma Buğdaycı Başal ◽  
Ayşe Durnalı
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Case ◽  
Early Stage ◽  
Medullary Carcinoma ◽  
Review Of The Literature ◽  
Rare Case Report

A case of 64-year-old female patient with early stage gastric medullary carcinoma has been presented, along with a review of the literature.

A symptomatic venous anomaly of the parotid gland: Case report and review of the literature

1988 ◽  
Vol 102 (6) ◽  
pp. 565-567 ◽  
Author(s):  
Johannes J. Manni ◽  
Johannes L. Merx ◽  
Paul van den Broek ◽  
Henk O. M. Thussen
Keyword(s):  
Case Report ◽  
Surgical Treatment ◽  
Parotid Gland ◽  
Female Patient ◽  
Rare Case ◽  
Definitive Diagnosis ◽  
Venous Anomaly ◽  
Review Of The Literature

Abstract A rare case of a symptomatic venous anomaly of the parotid gland is described in a 14-year-old female patient who presented with Turkey Wattle sign. A definitive diagnosis of this disorder requires venographic studies. Surgical treatment was successful, with a follow-up of four years.

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