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 ◽  
...  
2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Ferit Aslan ◽  
Fisun Ardıç Yükrük ◽  
Fatma Buğdaycı Başal ◽  
Ayşe Durnalı

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

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.


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.


2022 ◽  
Vol 8 ◽  
Author(s):  
Wen Chun Chen ◽  
Tie hao Wang ◽  
Ding Yuan ◽  
Ji Chun Zhao

Background: Multiple splenic artery aneurysms (MSAAs) are rare and there are few reports about their treatment. We herein present a rare case of MSAAs treated with splenectomy combined with endovascular embolization.Methods: A 51-year-old female patient was incidentally diagnosed with MSAAs. Splenectomy combined with endovascular embolization was the chosen treatment.Outcomes: The patient recovered uneventfully and was discharged from the hospital 5 days after splenectomy. The patient has been doing well during the 27-months of follow-up.Conclusion: Combined with the experience of the previous literature, we think splenectomy combined with endovascular embolization is a safe, reliable and minimally invasive treatment for some selected multiple SAAs, depending on several patient parameters, such as the age, sex, aneurysm dimension, aneurysm location, complications, and severity of the clinical findings.


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