Dangerous interaction of bitter melon (Momordica charantia) with pazopanib: A case of acute pancreatitis

2021 ◽  
pp. 107815522110407
Author(s):  
Oktay Unsal ◽  
Osman Sütcüoğlu ◽  
Ozan Yazıcı

Introduction Acute pancreatitis associated with Pazopanib has been reported in the literature. Bitter Melon (Momordica Charantia) is traditionally used as a folk medicine in many regions. In this report, we describe a 65-year-old patient with a diagnosis of renal cell carcinoma, admitted to the hospital with symptoms of acute pancreatitis at the 8th year of pazopanib treatment. Case Report The patient diagnosed with renal cell carcinoma was admitted to the hospital with the complaint of abdominal pain, nausea, and vomiting in the 8th year of Pazopanib treatment. It was noticed from the patient's history that he had received Bitter Melon extract for 4 days prior to the beginning of his complaints (100–150 ml/day). Levels of serum amylase and lipase were measured as 9163 U/L and 14,206 U/L, respectively. Management & Outcome Pazopanib drug was held. The patient was treated for acute pancreatitis. Pazopanib treatment was started again after the clinical condition of the patient had improved and levels of serum amylase and lipase had returned to normal levels. Levels of serum amylase and lipase did not increase again after re-administration of pazopanib treatment. Discussion It is thought that Bitter Melon extract and pazopanib interaction might have led to acute pancreatitis. To the best of our knowledge, this case is the first to highlight the interaction of Bitter Melon extract with pazopanib. The Drug Interaction Probability Scale indicates that there is a probable association between bitter melon and acute pancreatitis.

1983 ◽  
Vol 22 (4) ◽  
pp. 265-268 ◽  
Author(s):  
Joseph M. Klausner ◽  
Roland R. Rozin ◽  
Shlomo Lelcuck ◽  
Bianka Ilie

2002 ◽  
Vol 68 (3) ◽  
pp. 202-203 ◽  
Author(s):  
G. Nabi ◽  
P.N. Dogra ◽  
Ashmeet Chowdhary

2012 ◽  
Vol 2012 ◽  
pp. 1-4
Author(s):  
Rahul G. Matnani ◽  
Roshan K. Patel ◽  
Stephen E. Strup ◽  
Rouzan G. Karabakhtsian

A 69-year-old Caucasian female, with a previous diagnosis of 5q minus myelodysplastic syndrome, presented with conventional renal cell carcinoma (RCC) associated with multiple-epithelioid nonnecrotizing granulomas. Two previous reports of sarcoidosis, primarily involving the lung and skin, have been described in patients with 5q minus myelodysplasia. A cluster of closely linked genes encoding for cytokines such as IL-4, IL-5, and IL-3 are present on chromosome 5q. Hence, in sarcoidosis, cytokine imbalances associated with the deletion of these cytokine genes have been postulated. However, an occurrence of epithelioid granulomas within a carcinoma, in preexisting clonal myelodysplastic syndrome, has not been described. The patient, in the current study, had long standing 5q minus deletion, clinically characterized by refractory anemia associated with hypolobated megakaryocytes. However, the patient's history was negative for sarcoidosis and the extensive nonnecrotizing epithelioid granulomas were confined within RCC. Due to the absence of Th-2 cytokines, such as IL-4 and IL-5, in a subset of 5q minus myelodysplastic syndrome, proinflammatory Th-1 cytokines such as IFN-γand TNF-αmay be exaggerated in an environment conducive to antigen expression. Hence, we propose a greater susceptibility for the development of granulomas, at least in a subset of patients with 5q minus myelodysplasia.


2016 ◽  
Vol 2 (2-3) ◽  
pp. 63-65 ◽  
Author(s):  
Utku Oflazoglu ◽  
Umut Varol ◽  
Ahmet Alacacioglu ◽  
Tarik Salman ◽  
Necla Demir ◽  
...  

2009 ◽  
Vol 42 (12) ◽  
pp. 1837-1842
Author(s):  
Toshimichi Asano ◽  
Kazuhiro Iwai ◽  
Kazuaki Hazama ◽  
Ryosuke Kawasaki ◽  
Seiji Mega

2019 ◽  
Vol 23 (2) ◽  
pp. 108-111
Author(s):  
Guy Sydney ◽  
Kalliopi Ioakim ◽  
Nayia Kara ◽  
George Pantelas

Summary Backgroung/Aim: Salivary gland malignancies are rare, with only a fraction due to metastases. We report a rare case of the Clear Cell Renal Cell Carcinoma (CCRCC), a subtype of the Renal Cell Carcinoma (RCC), metastasizing to the parotid gland more than five years following nephrectomy. Case report: A 75-year-old female presented with a unilateral left parotid mass that was growing over the period of 18 months. After clinical and laboratory examinations, the patient underwent left partial superficial parotidectomy with preservation of the facial nerve. The significance of the patient’s history of the CCRCC was pivotal to the histopathological diagnosis of a metastatic CCRCC to the parotid. Conclusions: The unpredictable nature of the RCC results in the need for a long period of follow-up, as well as having a high degree of suspicion of metastasis in a patient presenting with a medical history of the RCC and a parotid mass.


1983 ◽  
Vol 130 (4) ◽  
pp. 829-829
Author(s):  
J.M. Klausner ◽  
R.R. Rozin ◽  
S. Lelcuck ◽  
B. Ilie

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