scholarly journals Isolated duodenal varices as the initial presentation of hepatocellular carcinoma

2013 ◽  
Vol 2013 (dec17 1) ◽  
pp. bcr-2013-201470-bcr-2013-201470 ◽  
Author(s):  
A. Okoli ◽  
P. Raymond ◽  
N. Ammannagari ◽  
N. Merrell
2014 ◽  
Vol 2014 ◽  
pp. 1-5
Author(s):  
Irappa Madabhavi ◽  
Apurva Patel ◽  
Mukesh Choudhary ◽  
Suhas Aagre ◽  
Swaroop Revannasiddaiah ◽  
...  

Hepatoblastoma (HB) is a rare malignant tumour of the liver and usually occurs in the first three years of life. Hepatoblastoma in adolescents and young adults is extremely rare; nevertheless the prognosis is much worse than in childhood, because these kinds of tumours are usually diagnosed late. Characteristic imaging and histopathological and AFP levels help in the diagnosis of hepatoblastoma. Paraneoplastic features of hepatoblastoma are not uncommon at presentation and include erythrocytosis, thrombocytosis, hypocalcaemia, isosexual precocious puberty, and rarely hypoglycaemia. Even though hypoglycaemia is commonly seen in hepatocellular carcinoma, its association with hepatoblastoma is very rare. We present a case of 15-year-old male patient presenting with complaints of recurrent hypoglycaemic seizures ultimately leading to diagnosis of hepatoblastoma. Managed successfully with neoadjuvant chemotherapy, surgery and adjuvant chemotherapy with adriamycin and cisplatin based regimens. An extensive review of literature in the PubMed and MEDLINE did not reveal much data on paraneoplastic recurrent hypoglycaemic seizures as an initial presentation of hepatoblastomas in adolescents and young adults.


Thyroid ◽  
2005 ◽  
Vol 15 (12) ◽  
pp. 1399-1400 ◽  
Author(s):  
Fatih Tunca ◽  
Yasemin Giles ◽  
Mine Güllüoǧlu ◽  
Yasemin Özlük ◽  
Tarık Terzioǧlu ◽  
...  

2017 ◽  
Vol 4 (1) ◽  
pp. e72
Author(s):  
Derek B. Laskar ◽  
Ghulam Ilyas ◽  
Daniel Diaz ◽  
Charles Shao

Author(s):  
Chetan Kalal ◽  
Adinath Wagh ◽  
Atif Patel ◽  
Harshad Joshi ◽  
Ravindra Surude ◽  
...  

Cranial metastases from hepatocellular carcinoma (HCC) has been seldom reported. Reported herein is the case of a painless parietal bone mass as an initial presentation of HCC in a 63-year-old female patient who was subsequently diagnosed to have HCV related cirrhosis. The biopsy from cranial lesion was confirmatory of HCC on immunohistochemistry. The patient had no known history of chronic liver disease. The presented diagnosis was made through detailed history, laboratory parameters and cross sectional imaging.


2014 ◽  
Vol 109 ◽  
pp. S385-S386
Author(s):  
Yana Cavanagh ◽  
Nihar Shah ◽  
Hamid Shaaban ◽  
Allison Thomas ◽  
Walid Baddoura ◽  
...  

2016 ◽  
Vol 6 (1) ◽  
pp. 16-19
Author(s):  
Sonal Saran ◽  
Pushpinder Singh Khera ◽  
Rengarajan Rajagopal ◽  
Neeraj Mehta ◽  
Poonam Elhence

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