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Hodgkin lymphoma case study ppt

James R. Stier, Robert J. A three-year-old boy presented with an enlarging neck mass. The patient received cyclophosphamide, doxorubicin, vincristine, and prednisone CHOP with rituximab and had excellent results. NLPHL is a B-cell malignancy likely of germinal center origin that has an overall good prognosis and favorable response to treatment.
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Hodgkin's lymphoma presenting with heart failure: a case report

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Non-Hodgkin's lymphoma with uncommon clinical manifestations: A case report

In and Carl Sternberg and. Therefore, it concluded that excision biopsy is accurate in assessing a patient who presents with symptoms suggestive of Hodgkin lymphoma. As this case study reportsa histologic diagnosis of Hodgkin lymphoma is always required. He studied seven individuals with painless lymph node enlargement.
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Childhood Hodgkin Lymphoma Treatment (PDQ®)–Health Professional Version

Although epitrochlear lymph nodes may be enlarged as a part of generalized lymphadenopathy, isolated enlargement of epitrochlear lymph nodes is rarely seen. We describe Hodgkin's lymphoma in a year-old male who presented with isolated epitrochlear lymphadenopathy of his right arm. In the histopathological examination of the epitrochlear lymph node was a lymphocyte-rich Hodgkin lymphoma with a clinical grade CS IA diagnosed. Epitrochlear lymph node involvement, as a first presentation, is rarely seen in Hodgkin's lymphoma. The aim of this study was to recapitulate the possible background diseases arising on the basis of an asymptomatic epitrochlear lymphadenopathy, to review the Hodgkin lymphoma presenting with primary epitrochlear lymphadenopathy in light of the literature, and to highlight the importance of a careful examination of the elbow site in routine physical examination.
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Moreover, to the best of our knowledge, primary retroperitoneal lymphoma without renal and ureteral involvement affecting the genitourinary system has not been reported until now. Here, we report the extremely rare case of a young female suffering with primary DLBCL located in the retroperitoneal and gastrointestinal region simultaneously. Unusually, the first symptom of this disease was renal colic.
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