scholarly journals An unusual case of diffuse large B‐cell lymphoma complicating a Crohn's disease

2020 ◽  
Vol 8 (12) ◽  
pp. 3062-3065
Author(s):  
Meriam Sabbah ◽  
Fatma Ben Farhat ◽  
Nawel Bellil ◽  
Fatma Khanchel ◽  
Asma Ouakaa ◽  
...  
2019 ◽  
Vol 13 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Koichi Sato ◽  
Tomoaki Suga ◽  
Atsuhiro Hirayama ◽  
Seiichi Daikuhara ◽  
Takeshi Uehara ◽  
...  

2020 ◽  
Vol 13 (4) ◽  
pp. e228818 ◽  
Author(s):  
Adam Joseph Hardy ◽  
Ionica Stoica ◽  
David Edward Kearney ◽  
Diarmuid S O'Riordain

A 62-year-old man presented to our institute with diarrhoea and dysuria on a background of subtotal colectomy and end ileostomy and biological therapy for Crohn’s disease. He was diagnosed with urinary tract infection and acute kidney injury (AKI). Renal ultrasound suggested left hydronephrosis, with renal protocol computed tomography (CT) showing a large pelvic mass. Magnetic resonance imaging (MRI) of the pelvis demonstrated a rectal tumour invading the bladder and compressing both ureters. He underwent cystoscopy, flexible sigmoidoscopy and positron emission tomography–CT and was diagnosed with stage IV non-Hodgkin’s diffuse large B-cell lymphoma. He was treated primarily with rituximab, cyclophosphamide, hydroxydaunomycin, oncovin and prednisolone chemotherapy regimen. He had ongoing urosepsis before admission for pelvic exenteration. He underwent cystoprostatectomy, excision of rectal stump and formation of ileal conduit. Histology showed no signs of residual malignancy. One year later, the patient was admitted to the intensive care unit with aspiration pneumonia, urosepsis and AKI. Despite maximal therapy, he developed multiorgan failure and passed away.


2015 ◽  
Vol 65 (4) ◽  
pp. 241 ◽  
Author(s):  
Tae Hyoung Koo ◽  
Won Jong Choi ◽  
Seung Hee Han ◽  
Su Young Kim ◽  
Jong Hun Lee

2014 ◽  
Vol 39 (10) ◽  
pp. e439-e441
Author(s):  
Giorgio Treglia ◽  
Gaetano Paone ◽  
Ulrike Perriard ◽  
Luca Ceriani ◽  
Luca Giovanella

CytoJournal ◽  
2018 ◽  
Vol 15 ◽  
pp. 2
Author(s):  
Prajwala Gupta ◽  
Poojan Agarwal ◽  
Arvind Ahuja ◽  
C. K. Durga

Primary cutaneous B-cell lymphomas (PCBCL) are a heterogeneous group of neoplasms with distinct biology and clinical course when compared to their nodal counterparts. They usually present as violaceous, erythematous plaques, and nonulcerated nodules, which are confined to skin at the time of presentation. We present an unusual case of primary cutaneous diffuse large B-cell lymphoma, clinically mimicking a sarcoma. This case highlights the uncommon aggressive behavior and ulcerated type of nodular lesions seen in PCBCL and also revisits the cytomorphological findings of the same.


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