scholarly journals Recurrent hepatic sarcoidosis post-liver transplantation manifesting with severe hypercalcemia: A case report and review of the literature

2005 ◽  
Vol 11 (12) ◽  
pp. 1611-1614 ◽  
Author(s):  
Cem Cengiz ◽  
Manuel Rodriguez-Davalos ◽  
Graciela deBoccardo ◽  
M. Isabel Fiel ◽  
Gonzalo Rodriguez-Laiz ◽  
...  
2020 ◽  
Vol 7 (07) ◽  
pp. 4871-4874
Author(s):  
Amal Hajri ◽  
Abdessamad El Azhary ◽  
Driss Erguibi ◽  
Rachid Boufettal ◽  
Saad Rifki El Jai ◽  
...  

Primary anorectal malignant melanoma is an extremely rare condition. It appears at the third highest frequency after melanomas of the skin and retina. Its prognosis is dreadful because of the early onset of metastases. The treatment remains essentially surgical. We report an observation of primitive anorectal melanoma, collected at the department of surgery for digestive cancers and liver transplantation of the Ibn Rochd University Hospital of Casablanca, with a review of the literature. In order to analyse the clinical, paraclinical and therapeutic characteristics of primary anorectal melanoma.


Author(s):  
Pietro PERDUCA ◽  
Daniel Reis WAISBERG ◽  
Rafael Soares Nunes PINHEIRO ◽  
Eduardo Guimarães HOURNEAUX-DE-MOURA ◽  
Luiz Augusto Carneiro D’ALBUQUERQUE ◽  
...  

2018 ◽  
Vol 12 (1) ◽  
Author(s):  
Pongprueth Rujirachun ◽  
Apichaya Junyavoraluk ◽  
Weerapat Owattanapanich ◽  
Voraparee Suvannarerg ◽  
Sirinart Sirinvaravong

2021 ◽  
Author(s):  
J Sollors ◽  
B Kallinowski ◽  
T Gaiser ◽  
C Antoni ◽  
M Ebert ◽  
...  

2006 ◽  
Vol 130 (1) ◽  
pp. 93-96
Author(s):  
Joan E. Etzell ◽  
Endi Wang

Abstract Pelger-Huët anomaly is a congenital or acquired abnormality of neutrophil nuclear segmentation. The acquired form may be a result of a clonal myeloid malignancy, such as myelodysplastic syndrome, or may be a secondary nonclonal change related to a variety of underlying causes, including infections and medications. We report a case of a 56-year-old man who developed acquired Pelger-Huët anomaly following liver transplantation while on the immunosuppressive agents tacrolimus and mycophenolate mofetil. These medications have been reported in association with this abnormality, but usually as a single agent or in combination with other drugs. In our case, the Pelger-Huët anomaly may be the result of the combination of these 2 drugs or mycophenolate alone with subsequent desensitization because resolution of the abnormality occurred after a reduction in mycophenolate mofetil dose, and the abnormality did not recur when mycophenolate mofetil was increased to a dose previously associated with Pelger-Huët anomaly during the time that tacrolimus was discontinued.


Vascular ◽  
2019 ◽  
Vol 28 (2) ◽  
pp. 165-171
Author(s):  
Jun Jie Ng ◽  
Jarrod Kah Hwee Tan ◽  
Julian Chi Leung Wong ◽  
Bernard Boon Kee Wee ◽  
Iyer Ganpathi Shridhar ◽  
...  

Background Mycotic vascular complications after liver transplantation are rare but can be pose a serious threat to the liver graft and the patient’s life. Mycotic complications can present as an incidental finding on routine imaging, or as haemorrhagic shock. Traditionally, these mycotic vascular complications were managed with open surgery. Method/results In this case report, we describe a patient who had developed multiple sequential mycotic aneurysms after liver transplantation which were managed successfully using endovascular and percutaneous techniques. Conclusion An endovascular approach is minimally invasive and will be the way forward in managing these mycotic vascular complications.


2020 ◽  
Vol 8 (12) ◽  
pp. 3008-3012
Author(s):  
Igor Lepski Calil ◽  
Francisco Tustumi ◽  
Rafael Soares Nunes Pinheiro ◽  
Ryan Yukimatsu Tanigawa ◽  
Ruy Jorge Cruz Junior ◽  
...  

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