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

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).

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

Sao Paulo Medical Journal ◽

10.1590/s1516-31802012000200010 ◽

2012 ◽

Vol 130 (2) ◽

pp. 126-129 ◽

Cited By ~ 5

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.

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Malignant Urothelial Carcinoma of Urinary Bladder in a Young Child: A Rare Case Report

Urology ◽

10.1016/j.urology.2012.12.016 ◽

2013 ◽

Vol 81 (4) ◽

pp. 888-890 ◽

Cited By ~ 13

Author(s):

Sujoy Neogi ◽

Piaray Lal Kariholu ◽

Gaurav Dhakre ◽

Vishal Gupta ◽

Neema Agarwal ◽

...

Keyword(s):

Case Report ◽

Young Child ◽

Urinary Bladder ◽

Urothelial Carcinoma ◽

Rare Case ◽

Rare Case Report

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Urinary Bladder Cavernous Hemangioma in a 3-year-old: A rare case report.

10.22541/au.163937715.58370714/v1 ◽

2021 ◽

Author(s):

Charles Odongo ◽

raymond atwine ◽

Martin Situma ◽

ambrose okello ◽

eugene ogwang ◽

...

Keyword(s):

Case Report ◽

Urinary Bladder ◽

Cavernous Hemangioma ◽

Rare Case ◽

Embryonal Rhabdomyosarcoma ◽

Bladder Tumors ◽

Case Presentation ◽

Rare Case Report

Introduction: Cavernous hemangioma accounts for 0.6% of bladder tumors. We present a rare case Case Presentation: A 3-year-old girl presented with intravaginal swelling, dysuria, and hematuria. She received 26 cycles of VAC for embryonal rhabdomyosarcoma. Histopathology confirmed CH. Conclusion: CH should be considered in the differentials of childhood genitourinary masses.

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