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Your search keyword '"non Hodgkin"' showing total 7 results
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7 results on '"non Hodgkin"'

1. A rare case of Gingival Myeloid sarcoma in a child

Author

Meghashree Vishwanath, Purnima S Rao, and Muktha R Pai

Subjects
Burkitt, Intraoral, Lymphoma, Myeloid, Non Hodgkin, Sarcoma, Pathology, RB1-214
Abstract

Myeloid sarcoma is a rare tumour composed of immature myeloid cells. Its occurrence in childhood is rare. Only a few cases of intraoral myeloid sarcoma have been reported in literature. We present a case of myeloid sarcoma with simultaneous involvement of intraoral soft tissues and lymph node. Here, importance is given to suspect this frequently misdiagnosed disease.

Published
2017
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2. Linfoma no Hodgkin estadio IV con metástasis mamaria y vaginal.

Author

Cabistany-Esqué, A. C., Franco-Serrano, C., Guardia-Dodorico, L., Gabasa-Gorgas, L., Aragón-Sanz, M. A., and Martínez-Medel, J.

Subjects
HODGKIN'S disease, OSTEOARTHRITIS, VAGINAL cancer, POSTMENOPAUSE, LYMPHOMAS
Abstract

Copyright of Ginecología y Obstetricia de México is the property of Federacion Mexicana de Ginecologia y Obstetricia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Published
2018
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3. Un cas rare d'un lymphome non hodgkinien type B du sinus maxillaire.

Author

SABANI, Hicham, FIQHI, Kamal, ALLAOUI, Mohamed, and EL KHATIB, Karim

Abstract

Non-hodgkin lymphoma (NHL) are rare tumors of the jaws. their locations in the air spaces of the face coming in second row. We related the case of a primitive NHL located in the maxillary sinus in a patient of 47 years, which illustrates the diagnostic difficulties encountered face a little suggestive symptoms. The diagnosis was confirmed by histological examination. The evolution was favorable after medical treatment based chemotherapy combined with versatile external radiotherapy. From this observation, we will review the literature in order to review the clinical, radiological, histological, therapeutic and outcome of this rare disease. [ABSTRACT FROM AUTHOR]

Published
2017
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4. A Rare Case of Primary Extranodal Laryngeal Non Hodgkin Lymphoma.

Author

P., Mark, A., Najihah Hanim, O., Eshamsol Kamar, A., Suhaila, and M., Irfan

Subjects
*B cell lymphoma
Abstract

Lymphoma is generally a nodal disease and arises from lymphoid tissues or organs. Extranodal lymphoma accounts for almost a third of malignant lymphomas. Squamous cell carcinoma accounts for 90% of laryngeal carcinoma, while extranodal Non Hodgkin Lymphoma (NHL) attributes only less than 1% of laryngeal neoplasms. Less than 100 of such cases been reported in literature since 1952. As to our best knowledge, no such case was ever reported in our country. We report a case of a 58-year-old gentleman who presented the typical history of laryngeal malignancy however the pathology turned out to be as NHLof Diffuse Large B-cell subtype. [ABSTRACT FROM AUTHOR]

Published
2018

5. Primary intraosseous B-cell lymphoblastic lymphoma of the mandible: a case report.

Author

C. P., Caamaño Martínez, V. E., Palacios Inostroza, and E., Báez Rivas

Subjects
B cells, LYMPHOMAS, MANDIBLE, T cells, MOUTH tumors, CELL morphology
Abstract

Introduction: Lymphoblastic lymphoma (LBL) is a malignant neoplasm that originates from precursors of B or T lymphocytes and constitutes approximately 2% of all nonHodgkin lymphomas. They are infrequent in the oral cavity, even more so if it is an extra-nodal primary presentation. In this location, neither the clinical features nor the radiological appearance is pathognomonic and can represent significant diagnostic problems. Case Report: We present the case of a seven-year-old female patient with a slowly enlarging painless right mandibular mass of two weeks of evolution. Radiographic studies showed an infiltrative hypodense area involving the right mandibular body, compromised teeth in formation, and vestibular and lingual cortical. Histological examination revealed a malignant neoplasm with a proliferation of round, small, blue morphology cells. In addition, immunohistochemical markers for TdT and PAX5 were positive. The diagnosis was B-cell lymphoblastic lymphoma and complementary studies confirmed only mandibular involvement without infiltration to other organs. Conclusions: The presentation of this case seeks to describe a rare neoplasm in the oral cavity, including clinical and radiographic presentation, histological characteristics, and immunological profile. The importance of an early and accurate diagnosis of this entity is emphasized due to the impact on patient survival. [ABSTRACT FROM AUTHOR]

Published
2023

6. A rare case of Gingival Myeloid sarcoma in a child

Author

Purnima S Rao, Muktha R Pai, and Meghashree Vishwanath

Subjects
Myeloid, Pathology, medicine.medical_specialty, Lymphoma, business.industry, Soft tissue, Sarcoma, Disease, medicine.disease, Non Hodgkin, medicine.anatomical_structure, hemic and lymphatic diseases, Rare case, medicine, Myeloid sarcoma, lcsh:Pathology, Burkitt, business, Lymph node, Intraoral, lcsh:RB1-214
Abstract

Myeloid sarcoma is a rare tumour composed of immature myeloid cells. Its occurrence in childhood is rare. Only a few cases of intraoral myeloid sarcoma have been reported in literature. We present a case of myeloid sarcoma with simultaneous involvement of intraoral soft tissues and lymph node. Here, importance is given to suspect this frequently misdiagnosed disease.

Published
2017

7. Primary cutaneous B-cell lymphoma: Narrative review of the literature

Author

Nicola Pimpinelli, Stefano Cicchelli, Emilio Berti, Maria Teresa Fierro, Silvia Alberti Violetti, Roberta La Selva, Vieri Grandi, Pietro Quaglino, Paolo Fava, Chiara Delfino, and Alessandro Pileri

Subjects
medicine.medical_specialty, Lymphoma, B-Cell, Skin Neoplasms, Lymphoma, Lymphoproliferative disorders, Primary cutaneous B-cell lymphoma, Lymphoma B-cell, Marginal Zone, Dermatology, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, Diffuse Pattern, hemic and lymphatic diseases, medicine, Humans, Lymphoma, Follicular, B cell, Large B-cell, business.industry, B-Cell, Follicular, Lymphoma, B-Cell, Marginal Zone, Diffuse, Non Hodgkin, Lymphoma, Large B-Cell, Diffuse, medicine.disease, medicine.anatomical_structure, Monoclonal, Primary cutaneous marginal zone lymphoma, Narrative review, business
Abstract

Primary cutaneous B-cell lymphomas comprehend a group of lymphoproliferative disorders characterized by being monoclonal proliferations of B-cell primarily involving the skin. Despite being recognized as autonomous and distinct clinico-pathologic entities since the late 80s, their classification is still an ongoing matter of debate. At the moment, WHO classification recognizes three disorders: primary cutaneous marginal zone lymphoma, primary cutaneous follicle center lymphoma and primary cutaneous diffuse large b-cell lymphoma (leg type). Primary cutaneous diffuse large b-cell lymphoma (other) has been used to define rare cases which show histologically an infiltrate with diffuse pattern composed by large b-cell, but not fitting with criteria for follicle center lymphoma nor for primary cutaneous diffuse large b-cell lymphoma (leg type). Aim of this review was to briefly describe all recognized and provisional entities included in the primary cutaneous b-cell lymphomas and to discuss recent acquisitions that may influence their future classifications.

Published
2019

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