Surgical Treatment of Occlusion of the Infrarenal Abdominal Aorta

1987 ◽  
Vol 138 (3) ◽  
pp. 687-687
Author(s):  
P. Ketonan ◽  
P.-T. Harjola ◽  
K. Ala-Kulju ◽  
T. Mattila ◽  
R. Luosto ◽  
...  
2020 ◽  
Vol 28 (4) ◽  
pp. 506-513
Author(s):  
Alexander F. Kharazov ◽  
V. A. Kul'bak ◽  
Naida Minatullaevna Basirova

Aim. To demonstrate a case of treatment of a patient with a rare vascular anomaly hypoplasia of infrarenal abdominal aorta. On a clinical example of female patient U., 41 years of age, with critical ischemia of the lower limbs and diagnosis hypoplasia of the abdominal aorta made on the basis of the clinical and instrumental data, the manifestations, diagnostics and potentials of the successful surgical treatment of the given pathology were demonstrated. Conclusion. Clinical manifestations of hypoplasia of the aorta depend on localization of the lesion and involvement of renal arteries. The commonest clinical sign is arterial hypertension and symptoms associated with the elevated arterial pressure. Hypoplasia of the aorta may also be manifested by hypertrophy of the upper limbs in combination with poor development of muscles of the lower limbs. More aged individuals present with arterial insufficiency leading to clinically significant ischemia of the lower limbs. Thus, in the case described, the patient already had ischemic trophic ulcers of the lower limbs. Without treatment, secondary arterial hypertension and cardiac failure may lead a patient to early death. Today, irrespective of the etiology, the only effective method of treatment of this disease is surgery. In case of our patient, resection of the hypoplastic segment of the aorta and its prosthetics were performed. This permitted to restore circulation in the lower parts of the body and further led to complete healing of trophic ulcers of the shin and to normalization of the systemic arterial pressure.


2003 ◽  
Vol 17 (3) ◽  
pp. 277-283 ◽  
Author(s):  
Pierre Alric ◽  
Frédérique Ryckwaert ◽  
Marie-Christine Picot ◽  
Pascal Branchereau ◽  
Pascal Colson ◽  
...  

Surgery Today ◽  
2002 ◽  
Vol 32 (5) ◽  
pp. 418-420 ◽  
Author(s):  
Jorge Adalberto Flores ◽  
Toshiya Nishibe ◽  
Fabio Kudo ◽  
Jun-ichi Oka ◽  
Keiko Miyazaki ◽  
...  

2019 ◽  
pp. 293-306
Author(s):  
Alexis R. Powell ◽  
Gabriel Crowl ◽  
Vikram S. Kashyap

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
Pooja Kumari ◽  
Debendra Pattanaik ◽  
Claire Williamson

Introduction. Aortic involvement leading to aortitis in eosinophilic granulomatosis polyangiitis (EGPA) is infrequent, and only 2 cases have been reported so far in the literature. Even more so, aortic aneurysm, secondary to EGPA, has never been reported and remains a diagnostic and therapeutic challenge. Case Presentation. We present a 63-year-old Caucasian male patient with a prior diagnosis of EGPA presenting with abdominal pain, nausea, and loose stools to the emergency department. Physical examination showed periumbilical tenderness. He had no peripheral eosinophilia but had high C-reactive protein and procalcitonin levels. CT abdomen revealed a mycotic aneurysm involving the infrarenal abdominal aorta. The patient declined surgical repair initially and was treated with IV antibiotics only. Unfortunately, 24 hours later, the aneurysm ruptured, leading to emergent axillofemoral bypass surgery. Surgical biopsy showed aortitis, periaortitis, and active necrotizing vasculitis. Conclusion. Abdominal aneurysms should be considered a complication of EGPA, and earlier immunosuppressive therapy should be considered to prevent further complications.


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