scholarly journals Massive Upper Gastrointestinal Bleeding Caused by Diffuse Large B-Cell Lymphoma

2016 ◽  
Vol 2016 ◽  
pp. 1-2
Author(s):  
O. Telci Caklili ◽  
H. H. Mutlu ◽  
Y. Colak ◽  
E. Ozturk ◽  
D. Kosemetin Dover ◽  
...  

Massive upper gastrointestinal bleeding is a life-threatening emergency which needs urgent intervention. Hematological malignancies are very rare causes of this type of bleeding and they usually originate from duodenum. In this case we present a gastric diffuse large B-cell lymphoma (DLBCL) causing massive upper gastrointestinal system bleeding. A 77-year-old male patient was admitted to emergency clinic with hematemesis and hematochezia. In physical examination patient was pale and sweaty; his vitals were unstable with a heart rate of 110 per minute and a blood pressure of 90/50 mmHg. His hemoglobin level was found 7.5 g/dL and he was transfused with one unit of packed red blood cells. After his vitals were normalized, gastroscopy was performed showing mosaic pattern in corpus and antrum mucosa and multiple ulcers in various sizes, largest being approximately 2 cm in diameter, higher than mucosa covered with exude mostly on corpus and large curvature. Biopsy results were reported as DLBCL. Gastric mucosa is involved in most of the DLBCL cases. Although not listed as a common cause of massive gastrointestinal bleeding DLBCL can cause life-threatening situations mostly because of its malignant nature.

2012 ◽  
Vol 107 ◽  
pp. S284
Author(s):  
Vipin Mittal ◽  
Gautamy Dhadham ◽  
Elizabeth Butler ◽  
Lisa Inchani ◽  
Walid Baddoura

2019 ◽  
Vol 94 (1) ◽  
pp. 93-95
Author(s):  
Mimari Kanazawa ◽  
Takeshi Sugaya ◽  
Kazuhiro Takenaka ◽  
Kohei Tsuchida ◽  
Keiichi Tominaga ◽  
...  

JRSM Open ◽  
2021 ◽  
Vol 12 (3) ◽  
pp. 205427042098362
Author(s):  
Andrew Coppola ◽  
Chia Chey ◽  
Emma O’Donovan ◽  
Monira Rahman

Acute liver failure is a life-threatening condition commonly caused by drug-induced hepatotoxicity or viral hepatitides. However, there are a number of rarer causes such as haemophagocytic lymphohistiocytosis. Haemophagocytic lymphohistiocytosis is a syndrome of uncontrolled immune cell activation, triggered by infection or malignancy, which carries a high mortality. Whilst mild to moderate liver injury is commonly seen with haemophagocytic lymphohistiocytosis, acute liver failure has rarely been reported in adults. We present a case of a 74-year-old man with acute liver failure secondary to haemophagocytic lymphohistiocytosis triggered by undiagnosed large B-cell lymphoma. Initially treated for biliary sepsis, there was a delay in the diagnosis of haemophagocytic lymphohistiocytosis and despite initiating chemotherapy, he died soon after. This case highlights the importance of considering haemophagocytic lymphohistiocytosis as a rare cause of acute liver failure, as given the life-threatening potential of haemophagocytic lymphohistiocytosis, a prompt diagnosis may allow early initiation of chemotherapy for any chance of survival.


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