scholarly journals Colonic mucosa-associated lymphoid tissue (MALT) lymphoma: an important differential diagnosis for a slow-growing colonic polyp

Endoscopy ◽  
2014 ◽  
Vol 46 (S 01) ◽  
pp. E625-E625
Author(s):  
Rohit Anand ◽  
Shashank Garg ◽  
Ethan Dubin ◽  
Sudhir Dutta
2016 ◽  
Vol 47 (4) ◽  
pp. 1244-1260 ◽  
Author(s):  
Raphael Borie ◽  
Marie Wislez ◽  
Martine Antoine ◽  
Christiane Copie-Bergman ◽  
Catherine Thieblemont ◽  
...  

This general review sought to clarify the pathophysiological, diagnostic, prognostic, and therapeutic features of pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma.MALT lymphoma is the most common pulmonary B-cell lymphoma, which usually occurs in the context of acquired MALT. The disease is slow-growing with an asymptomatic chronic alveolar opacity visible on radiography. Diagnosis requires tissue samples that should be retrieved using minimally invasive techniques, such as bronchoscopy or computed tomography-guided biopsies. The pathophysiology includes cytogenetic abnormalities and autoimmune diseases, whereas an association with a chronic pulmonary infection is still suspected but not yet demonstrated. Disease prognosis is typically excellent and the current available treatments are discussed in this review, including the decision not to treat, surgery, and single- or double-agent chemotherapy.


2017 ◽  
Vol 2017 ◽  
pp. 1-4 ◽  
Author(s):  
Raja Chandra Chakinala ◽  
Khwaja F. Haq ◽  
Jonathan E. Barsa ◽  
Shantanu Solanki ◽  
Lavneet Chawla ◽  
...  

We present a case of colonic mucosa-associated lymphoid tissue (MALT) lymphoma in a 62-year-old woman diagnosed after a positive test for fecal occult blood.


2014 ◽  
Vol 13 (4) ◽  
pp. 490-492
Author(s):  
Shaakir Hasan ◽  
Aruna Turaka

AbstractObjectivePapillary thyroid carcinoma combined with thyroid mucosa-associated lymphoid tissue (MALT) lymphoma is exceedingly rare and there is no standard management.Case reportWe report a rare association of MALT lymphoma of thyroid in a 60-year-old woman with Hashimoto's thyroiditis along with an incidental focus of papillary carcinoma.ConclusionPatients with Hashimoto's thyroiditis are prone to develop other thyroid pathology, including rare tumours such as MALT lymphoma. The differential diagnosis for a neoplasm in such patients should be wide.


2016 ◽  
Vol 83 (5) ◽  
pp. AB367-AB368
Author(s):  
Jacob A. Petrosky ◽  
Solomon O. Agbroko ◽  
XiuLi Liu ◽  
Robert Dean ◽  
James M. Church ◽  
...  

2020 ◽  
Vol 17 (2) ◽  
pp. 290-294
Author(s):  
G. I. Krichevskaya ◽  
E. S. Vakhova ◽  
S. V. Saakyan ◽  
E. B. Myakoshina ◽  
A. E. Andryushin ◽  
...  

Conjunctival lymphomas are predominantly extranodal B-cell non-Hodgkin’s lymphomas (NHL), most of them are MALT-lymphomas originating from the mucosa-associated lymphoid tissue. Manifestations of the conjunctival NHL are very diverse, and often imitate the appearance of other ocular diseases, which makes their clinical diagnosis difficult and significantly lengthens the time from the first visit to the ophthalmologist until the diagnosis is verified. The article presents the case histories of two young patients who were treated for a long time at the place of residence as acute chlamydial conjunctivitis (in one case — 3, in the other — almost 5 months). A comprehensive laboratory study to detect specific blood antibodies, DNA of the pathogen in conjunctival scrapings and the cytological picture of the conjunctiva did not confirm the chlamydial etiology of the process. A pronounced lymphoid reaction mainly due to small lymphoid cells was found in both patients in scrapings from the conjunctiva of the eyelid, which was the basis for referring patients for consultation to oncologist. Histological examination of conjunctival biopsy specimens also revealed proliferation of lymphoid tissue: patients with suspected MALT lymphoma were referred to onco-hematologists. A PCR analysis of the biopsy material revealed HHV-8 DNA in one patient and Epstein-Barr (EBV) DNA in another, although no pathogen genomes were detected in the conjunctiva scrapings. Immunohistochemical analysis in one patient confirmed the conjunctival MALT-lymphoma, in another one diagnosed hyperplasia of the conjunctival mucous-associated lymphoid tissue, caused by prolonged antigenic stimulation (EBV DNA was detected in the biopsy). The follicular appearance of the lymphocyte hyperplasia in conjunctiva may imitate the clinical picture of infectious diseases. For differential diagnosis of chlamydial conjunctivitis and MALTlymphoma, especially in young patients with refractory follicular conjunctivitis, it is advisable to include a set of serological, molecular biology and cytological methods.


2018 ◽  
Vol 2018 ◽  
pp. 1-3 ◽  
Author(s):  
Monjur Ahmed

Colonic MALToma accounts for 2.5% of all MALTomas. MALToma can be associated with certain chronic infections, autoimmune disorders, Waldenstrom’s macroglobulinemia, and old age. Synchronous MALTomas can occur in multiple organs. Simultaneous occurrence of colonic MALToma and colon cancer has been reported. A case of colonic MALToma and lung cancer is described here.


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