Successive xanthogranulomatous prostatitis after complete remission of metastatic prostate adenocarcinoma: An extremely rare case report with review of literatures

Rhabdomyosarcoma is a malignancy of mesenchymal tissue origin typically occurring in childhood and adolescence, with an incidence rate of of 4.3 patients per million population per anum. Primary rhabdomyosarcoma of para-testicular origin is an infrequent condition, making up to 7% of all the cases of rhabdomyosarcoma tumors in children and adolescents. Here we describe a case of a 25 years old man with left paratesticular solid mass. He underwent left sided orchiectomy with histopathology revealing paratesticuler embryonal rhabdomyosarcoma. He underwent definitive chemo-radiotherapy and orchidopexy with complete remission and is on active surveillance for 4 years.

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Coexisting prostate adenocarcinoma with multiple myeloma: A rare case report

Indian Journal of Pathology and Microbiology ◽

10.4103/ijpm.ijpm_591_17 ◽

2018 ◽

Vol 61 (3) ◽

pp. 434

Author(s):

Yelda Vyas ◽

Akanksha Salkar ◽

AKalpana Bothale

Keyword(s):

Multiple Myeloma ◽

Case Report ◽

Rare Case ◽

Prostate Adenocarcinoma ◽

Rare Case Report

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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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