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1.
BMC Urol ; 23(1): 191, 2023 Nov 18.
Artigo em Inglês | MEDLINE | ID: mdl-37980517

RESUMO

BACKGROUND: Ectopic kidney and median arcuate ligament syndrome are both rare conditions. The clinical presentation and diagnosis of these conditions are not well studied. There are no reports on the combination of these two rare conditions. CASE PRESENTATION: We report a 24-year-old woman with fever, dysuria, urinary frequency and left flank pain for two days. The primary diagnoses in the clinic were left acute pyelonephritis and left hydronephrosis due to throbbing pain in the left costovertebral angle and pyuria. However, further computed tomography showed right ectopic pelvic kidney, left renal pelvis dilatation without definite ureteral lesion, good bilateral renal contrast enhancement, and compression of the celiac axis due to obstruction by the median arcuate ligament. Chronic abdominal symptoms were reported by the patient after repeat history taking. The patient's condition was fully explained and discussed with her and her family, but they refused further therapy. After the acute pyelonephritis began improving, the patient was discharged for follow-up at our outpatient clinic. CONCLUSION: We present an extremely rare case of a combination of two rare conditions: ectopic kidney and median arcuate ligament syndrome. No study to date has reported on the relationship between the two diseases. Given the rarity of the two conditions, no evidence or even a hypothesis exists to explain the possible etiology of their combination. More reports are required to enhance the understanding of these rare conditions.


Assuntos
Nefropatias , Síndrome do Ligamento Arqueado Mediano , Pielonefrite , Feminino , Humanos , Adulto Jovem , Artéria Celíaca/patologia , Rim , Nefropatias/diagnóstico por imagem , Ligamentos/diagnóstico por imagem , Síndrome do Ligamento Arqueado Mediano/diagnóstico , Síndrome do Ligamento Arqueado Mediano/patologia
3.
Ann Diagn Pathol ; 52: 151732, 2021 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-33798927

RESUMO

Median Arcuate Ligament Syndrome (MALS) is a rare entity characterized by severe post-prandial epigastric pain, nausea, vomiting, and/or weight loss. Symptoms have been attributed to vascular compression (celiac artery compression syndrome, CACS), but it remains controversial whether they could be secondary to neural compression. Literature review identified rare description of pathologic findings in surgery journals. The clinico-pathologic findings of four MALS patients who underwent robotic or laparoscopic surgery in our hospital are described. All our patients were female with a median age of 32.5 (range 25-55 years), and a median BMI of 23.5 kg/m2. They presented with chronic often post-prandial abdominal pain (4/4), nausea (3/4), emesis (2/4), anorexia (1/4), and weight loss (1/4). Two patients had a history of Crohn's disease. At intraoperative exploration, the celiac artery and adjacent nerves and ganglia were encased and partially compressed by fibrotic tissue in each patient. In each case laparoscopic excision of fibrotic tissue, celiac plexus and ligament division and was performed; celiac plexus nerve block was also performed in one patient. After surgical intervention, symptoms improved in three of the patients whose specimens show periganglionic and perineural fibrosis with proliferation of small nerve fibers. Our findings support neurogenic compression as a contributing factor in the development of pain and other MALS symptoms, and favor the use of MALS rather than CACS as diagnostic terminology. To further study the pathogenesis of this unusual syndrome, surgeons should submit all tissues excised during MALS procedures for histopathologic examination.


Assuntos
Artéria Celíaca/patologia , Plexo Celíaco/patologia , Fibrose/patologia , Gânglios Simpáticos/patologia , Síndrome do Ligamento Arqueado Mediano/patologia , Dor Abdominal/etiologia , Adulto , Índice de Massa Corporal , Artéria Celíaca/cirurgia , Plexo Celíaco/cirurgia , Constrição Patológica/etiologia , Feminino , Fibrose/cirurgia , Gânglios Simpáticos/cirurgia , Humanos , Laparoscopia/métodos , Síndrome do Ligamento Arqueado Mediano/diagnóstico , Síndrome do Ligamento Arqueado Mediano/cirurgia , Pessoa de Meia-Idade , Náusea/etiologia , Bloqueio Nervoso/métodos , Avaliação de Resultados em Cuidados de Saúde , Período Pós-Prandial , Procedimentos Cirúrgicos Robóticos/métodos , Vômito/etiologia , Redução de Peso
4.
J Ultrasound ; 24(3): 317-321, 2021 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-31925730

RESUMO

Dunbar syndrome, also known as median arcuate ligament syndrome, is a rare clinical condition due to the external compression of the celiac trunk by the median arcuate ligament causing abdominal angina. We report a case of Dunbar syndrome and its borderline imaging findings focused on the crucial diagnostic role of color-Doppler ultrasound. We also reviewed the current literature, delineating the clinical manifestations and the diagnostic workup of the Dunbar syndrome with the objective to increase the knowledge of this clinical entity as a cause of postprandial abdominal pain and to underline the pivotal role of color-Doppler ultrasound to avoid incorrect or delayed diagnosis.


Assuntos
Síndrome do Ligamento Arqueado Mediano , Dor Abdominal/diagnóstico por imagem , Dor Abdominal/etiologia , Adulto , Artéria Celíaca/diagnóstico por imagem , Constrição Patológica/diagnóstico por imagem , Feminino , Humanos , Síndrome do Ligamento Arqueado Mediano/diagnóstico por imagem , Síndrome do Ligamento Arqueado Mediano/patologia , Ultrassonografia Doppler em Cores
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