Lymphoma Flashcards

1
Q

What is the classic histologic halmark of Hodgkin disease?

A

Hodgkin lymphoma is defined by the presence of Reed-Sternberg cells, which are multinucleated large cells (“owl’s eyes”) that divide rapidly and live longer than normal cells. *** Image 24-25

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2
Q

What are the three subtypes of non-Hodgkin lymphoma?

A

Burkitt lymphoma, lymphoblastic lymphoma, and large cell lymphoma.

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3
Q

What (4) features, if present in conjunction with lymphadenopathy, would be worrisome for the presence of lymphoma?

A

Systemic symptoms (fever, night sweats, weight loss, etc.); fixed, nontender nodes; supraclavicular nodes; and lymph nodes > 2cm with no response to a 2 week course of antibiotics.

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4
Q

How is lymphoma diagnosed?

A

Biopsy of the worrisome lymph node or mass.

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5
Q

Within what age range is the incidence of Hodgkin lymphoma highest?

A

The highest incidence is seen in adolescents between 15 and 19 years of age.

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6
Q

T/F: Hodgkin disease is mostly of B cell lineage.

A

True. Although T-cell lineage is occasionally noted.

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7
Q

What is the most common presentation for Hodgkin disease?

A

The most common presentation for Hodgkin lymphoma is asymptomatic lymphadenopathy, which often involves the cervical or supraclavicular region.

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8
Q

What are “B” symptoms in Hodgkin disease? What does their presence usually indicate?

A

Fever, drenching night sweats, and unexplained weight loss. The presence of B symptoms usually indicates a more advanced disease and a worse prognosis.

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9
Q

What infection is common in patients with Hodgkin lymphoma, due to their impaired cellular immunity?

A

Varicella Zoster

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10
Q

What does ingestion of alcohol cause in a patient with Hodgkin disease?

A

It can cause alcohol-induced pain localized to areas of disease involvement (bones, lymph nodes, etc.).

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11
Q

How do you definitively diagnose Hodgkin disease?

A

Excisional biopsy of an accessable lymph node.

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12
Q

T/F: A staging laparotomy is routinely performed in patients with Hodgkin disease.

A

False. Staging includes several laboratory and imaging studies, but does not include laparotomy.

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13
Q

In general, how are patients treated for Hodgkin disease?

A

The combination of radiation and chemotherapy was found to improve treatment outcomes in patients with Hodgkin lymphoma, compared with radiation alone.

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14
Q

What are the two multi-agent chemotherapy regimens used to treat Hodgkin lymphoma?

A

MOPP (nitrogen Mustard, vincristine (i.e. Oncovin), Procarbazine, and Prednisone) and ABVD (doxorubicin (Adriamycin), Bleomycin, Vinblastine, and Dacarbazapine).

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15
Q

What are the (2) treatment-related risks of MOPP chemotherapy in patients with Hodgkin lymphoma?

A

AML and infertility.

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16
Q

What are the (2) treatment-related risks of ABVD chemotherapy in patients with Hodgkin lymphoma?

A

Dose-dependent side effects of cardiomyopathy (doxorubicin) and pulmonary toxicity (bleomycin).

17
Q

What is the most common type of lymphoma in pediatrics?

A

Non-Hodgkin lymphoma. NHL accounts for 60% of pediatric lymphomas, with Hodgkin making up the other 40%.

18
Q

What is the male:female ratio for non-Hodgkin lymphoma?

A

Males outnumber females 3:1.

19
Q

What four conditions have a high rate of developing non-Hodgkin lymphoma?

A

Ataxia-telangiectasia, Wiskott-Aldrich syndrome, HIV, and other immunosuppressive diseases.

20
Q

What is the most common form of non-Hodgkin lymphoma in pediatrics in the U.S.?

A

The sporadic form of Burkitt lymphoma, which accounts for ~50% of pediatric non-Hodgkin lymphomas.

21
Q

In which anatomic location do most cases of Burkitt lymphoma originate in US patients?

A

90% of Burkitt-type lymphomas originate from relatively mature B-cells in Peyer patches within the GI tract, most commonly at the ileocecal junction.

22
Q

How do most children with Burkitt lymphoma present?

A

A majority of patients present with an abdominal mass or pain with nausea and vomiting.

23
Q

What is a common complication of Burkitt lymphoma?

A

Burkitt lymphoma is the fastest-growing malignant tumor (it can double in size in 2-3 days). Consequently, tumor lysis syndrome is common.

24
Q

What sites are commonly affected in lymphoblastic lymphoma?

A

Anterior mediastinum, cervical/supraclavicular/axillary nodes, and involvement of the liver, spleen, and kidneys.

25
Q

How does the lymphadenopathy of large cell non-Hodgkin lymphoma differ from that of the other forms of lymphoma?

A

The lymphadenopathy with large cell NHL is usually tender, which separates it from the other lymphomas.

26
Q

Describe the staging system for non-Hodgkin Lymphoma.

A

Staging is generally based on the volume of the tumor. Stage I: single tumor or anatomic node, excepting the mediastinum or abdomen. Stage II: ≥ 2 nodal areas on the same side of the diaphragm, 2 extranodal tumors on the same side of the diaphragm, or a resectable primary GI tumor. Stage III: involvement of both sides of the diaphragm, all mediastinal or intrathoracic tumors, all unresectable abdominal disease, and all paraspinal or epidural tumors. Stage IV: any CNS or bone marrow involvement.

27
Q

T/F: Radiation therapy is a major component of most therapy for non-Hodgkin lymphoma.

A

False. Radiation therapy is usually limited to CNS disease or emergency situations (airway obstruction).

28
Q

How is most non-Hodgkin lymphoma treated?

A

The mainstay is chemotherapy, with the typical regimen being CHOP (Cyclophosphamide, doxorubacin (Hydroxydaunorubicin), vincristine (Oncovin), and Prednisone).