scholarly journals Orbital Mucosa-Associated Lymphoid Tissue Lymphoma and Primary Cutaneous Classical Hodgkin Lymphoma: A Rare Case Report and Review of the Literature

2020 ◽  
Vol 2020 ◽  
pp. 1-4
Author(s):  
Nicole Yun ◽  
James Coggan ◽  
Ira Miller ◽  
Parameswaran Venugopal
Keyword(s):  
Case Report ◽  
Maintenance Therapy ◽  
Hodgkin Lymphoma ◽  
Malt Lymphoma ◽  
Lymphoid Tissue ◽  
Rare Case ◽  
Classical Hodgkin Lymphoma ◽  
Review Of The Literature ◽  
Rare Case Report ◽  
Left Neck

A 60-year-old woman was diagnosed with isolated mucosa-associated lymphoid tissue (MALT) lymphoma of the ocular adnexa and treated with two years of weekly rituximab for eight doses followed by rituximab maintenance. After nearly two years of maintenance therapy, she developed a tender, indurated mass on the left neck. Biopsy results were consistent with primary cutaneous classical Hodgkin lymphoma (PCCHL).

scholarly journals Isolated primary spinal mucosa-associated lymphoid tissue (malt) lymphoma: a rare case report

2020 ◽  
Vol 42 ◽  
pp. 46-47
Author(s):  
O. Ekinci ◽  
A. Dogan ◽  
M. Aslan ◽  
I. Aras ◽  
C. Demir
Keyword(s):  
Case Report ◽  
Malt Lymphoma ◽  
Lymphoid Tissue ◽  
Rare Case ◽  
Rare Case Report

Primary Mucosa-Associated Lymphoid Tissue (MALT) Lymphoma of the Urinary Bladder: A Rare Case Report

2013 ◽  
Vol 14 (3) ◽  
pp. 212-214 ◽  
Author(s):  
Nese Arzu Yener ◽  
Orhun Sinanoglu ◽  
Gulbuz Sezgin ◽  
Ahmet Midi ◽  
Sinan Ekici
Keyword(s):  
Case Report ◽  
Urinary Bladder ◽  
Malt Lymphoma ◽  
Lymphoid Tissue ◽  
Rare Case ◽  
Rare Case Report

scholarly journals Mucosa-associated lymphoid tissue lymphoma of the trachea: case report

2012 ◽  
Vol 130 (2) ◽  
pp. 126-129 ◽  
Author(s):  
Maria Elisa Ruffolo Magliari ◽  
Renata Telles Rudge de Aquino ◽  
Anna Luiza Lobão Gonçalves ◽  
Fábio Marioni ◽  
Fabíola del Carlo Bernardi ◽  
...  
Keyword(s):  
Case Report ◽  
Complete Remission ◽  
Malt Lymphoma ◽  
Lymphoid Tissue ◽  
Rare Case ◽  
Endoscopic Biopsy ◽  
Rare Case Report ◽  
History Of ◽  
One Year ◽  
Indolent Disease

CONTEXT: Mucosa-associated lymphoid tissue (MALT) lymphomas are most commonly found in the stomach, lungs, orbital soft tissue, salivary glands and thyroid. Involvement of the trachea is extremely rare. CASE REPORT: This report describes a rare case of MALT lymphoma of the trachea in a 71-year-old woman who presented with a one-year history of coughing, dyspnea, hoarseness and weight loss. There was an infiltrative lesion in the mid-trachea. The anatomopathological diagnosis was only made from the fifth endoscopic biopsy attempt. Immunochemotherapy consisting of rituximab, cyclophosphamide, vincristine and prednisone (R-COP) induced complete remission of the symptoms and endoscopic lesion. CONCLUSIONS: MALT lymphoma of the trachea is extremely rare and indolent disease. It has to be considered in the differential diagnosis of airway lesions. It is crucial to obtain an anatomopathological diagnosis from a specialized pathologist. Immunochemotherapy with R-COP induced complete remission of the disease.

scholarly journals Is it always Wilms’ tumor? Localized cystic disease of the kidney in an infant. An extremely rare case report and review of the literature

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Christos Kaselas ◽  
Charikleia Demiri ◽  
Vasilios Mouravas ◽  
Eleni Koutra ◽  
Kleanthis Anastasiadis ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Wilms Tumor ◽  
Pediatric Population ◽  
Benign Disease ◽  
Cystic Disease ◽  
Proper Treatment ◽  
Review Of The Literature ◽  
Rare Case Report ◽  
Renal Malignancies

Localized Cystic Disease of the Kidney (LCDK) is an extremely rare benign disease in pediatric population. Although its management is conservative and generally requires no treatment, the unfamiliarity with the disease can expose such patients to misdiagnosis as renal malignancies or uncertainty for proper treatment. We report such a case in an infant and review the current literature.

scholarly journals Dysgenetic Polycystic Disease of Minor Salivary Gland: A Rare Case Report and Review of the Literature

2017 ◽  
Vol 2017 ◽  
pp. 1-5
Author(s):  
N. Srikant ◽  
Shweta Yellapurkar ◽  
Karen Boaz ◽  
Mohan Baliga ◽  
Nidhi Manaktala ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Salivary Gland ◽  
Case Report ◽  
Rare Case ◽  
Minor Salivary Gland ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Lower Lip ◽  
Polycystic Disease ◽  
Rare Case Report

Polycystic (dysgenetic) disease of the salivary glands is a rare entity that has only recently been described in the literature. The disease is more commonly seen in females and majority of the cases have presented as bilateral parotid gland swellings. This case presenting in a 21-year-old male is the first of this unusual entity involving solely the minor salivary gland on the lower lip. This case report highlights the importance for the clinician to be aware of this differential diagnosis, when treating an innocuous lesion like a mucocele.

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