Papapanagiotou IK, Kalles V, Migklis K, Sgantzos M, Kaklamanos I, Mariolis-Sapsakos T.
Langer's axillary arch. Clin Case Rep. 2016;4(6):613.
AbstractLanger's axillary arch is usually asymptomatic and difficult to detect preoperatively. When present, it is important for surgeons operating in the axillary region, to identify correctly the relevant anatomy. Simple surgical division is curative and necessary in order to achieve exposure of the axillary contents, lymphatic dissection, and neurovascular preservation.
Konstantinou EA, Mariolis Sapsakos TD, Katsoulas TA, Velecheris D, Tsitsimelis D, Bonatsos G.
Persistent left superior vena cava leads to catheter malposition during PICC Port placement. J Vasc Access. 2016;17(2):e29-31.
AbstractINTRODUCTION: We present a case of peripherally inserted central catheter (PICC) port placement where the catheter had been malpositioned to the persistent left superior vena cava.
METHODS: Despite the obvious elevation of the P-wave signaling proximity of the catheter tip to the sinus node, the catheter was not in the desired location within the superior vena cava or the right atrium, because of the presence of a persistent left superior vena cava. Computed tomography was used in order to locate the catheter.
RESULTS: The catheter was located in the persistent left superior vena cava.
CONCLUSIONS: Malpositioning of the catheter in the persistent left superior vena cava occurs in 0.3%-0.5% of patients. The catheter was subsequently removed.
Zoulamoglou M, Flessas I, Zarokosta M, Piperos T, Kalles V, Tsiaousis I, Kaklamanos I, Sgantzos M, Mariolis-Sapsakos T.
Congenital peritoneal encapsulation of the small intestine: A rare case report. Int J Surg Case Rep. 2016;27:28-31.
AbstractINTRODUCTION: Peritoneal Encapsulation (PE) is a scarce congenital malformation, characterized by a supplementary peritoneal membrane that covers all or a part of the small intestine.
PRESENTATION OF CASE: PE was unexpectantly discovered in a young woman during laparotomy for bowel obstruction. There were no specific pre-operative indications of this malformation. The operation was uneventful.
DISCUSSION: PE is a very rare congenital anatomical anomaly that is difficultly identified pre-operatively. PE is mainly asymptomatic, but in some cases, like in the presented one, PE presents with small bowel obstruction. Surgeons should be aware of this malformation and suspect it when encountering a patient with small bowel obstruction without other etiological factors.
CONCLUSION: Knowledge of this peculiar congenital anomaly is pivotal, so that accurate diagnosis and appropriate management of it are direct and efficient.