Abstract:Primary non-Hodgkin's lymphoma of the cervix is a rare disease, of which a subgroup of follicular lymphoma constitutes only 8.5%. There is not an established treatment protocol neither for primary cervical lymphoma nor for its follicular subgroup. We presented a case with Ann Arbor stage IEA (Extra-nodal involvement and absence of weight loss, fever, night sweat) primary follicular lymphoma of the cervix. She was treated with chemotherapy followed by pelvic radiotherapy. Upon relapse with a nodal neck mass, sh… Show more
“…Rituximab was used in only five patients as the majority of patients were treated in the pre-monoclonal antibody era. [10][11][12] Both our patients received rituximab-CHOP and showed excellent responses with no evidence of disease at 20 and 19 months post-treatment. This suggests addition of immunotherapy in the form of rituximab is of value in improving response rates, as has been observed in other nodal lymphomas.…”
Section: Treatmentmentioning
confidence: 91%
“…To preserve reproductive function in young patients, combination chemotherapy alone has been advocated in some case reports. 12,17 Survival Disease-free survival in this review ranged from 5 months to 8 years. Vang et al study of 10 patients reported a very good 5-year survival rate of 83%.…”
Section: Treatmentmentioning
confidence: 99%
“…This is an extrapolation of the usual therapy of stage I ⁄ II NHL with involved field radiotherapy (IF-XRT) and chemotherapy. 12 Infertility is a major concern for patients treated with chemotherapy and pelvic radiotherapy. The two most commonly used regimens -CHOP (4-6 cycles) and cyclophosphamide, vincristine, prednisolone -have lower risk (<20%) of causing permanent infertility.…”
Primary lymphoma of the uterus and cervix is rarely encountered. We present two cases of diffuse large B-cell lymphoma of the cervix and uterus that were treated with R-CHOP chemotherapy followed by pelvic radiotherapy. The women are disease free 20 and 19 months after the diagnosis respectively. Seventy-two cases of primary uterine and cervical lymphoma reported in the English literature in the last 10 years from 2000 to 2010 are reviewed.
“…Rituximab was used in only five patients as the majority of patients were treated in the pre-monoclonal antibody era. [10][11][12] Both our patients received rituximab-CHOP and showed excellent responses with no evidence of disease at 20 and 19 months post-treatment. This suggests addition of immunotherapy in the form of rituximab is of value in improving response rates, as has been observed in other nodal lymphomas.…”
Section: Treatmentmentioning
confidence: 91%
“…To preserve reproductive function in young patients, combination chemotherapy alone has been advocated in some case reports. 12,17 Survival Disease-free survival in this review ranged from 5 months to 8 years. Vang et al study of 10 patients reported a very good 5-year survival rate of 83%.…”
Section: Treatmentmentioning
confidence: 99%
“…This is an extrapolation of the usual therapy of stage I ⁄ II NHL with involved field radiotherapy (IF-XRT) and chemotherapy. 12 Infertility is a major concern for patients treated with chemotherapy and pelvic radiotherapy. The two most commonly used regimens -CHOP (4-6 cycles) and cyclophosphamide, vincristine, prednisolone -have lower risk (<20%) of causing permanent infertility.…”
Primary lymphoma of the uterus and cervix is rarely encountered. We present two cases of diffuse large B-cell lymphoma of the cervix and uterus that were treated with R-CHOP chemotherapy followed by pelvic radiotherapy. The women are disease free 20 and 19 months after the diagnosis respectively. Seventy-two cases of primary uterine and cervical lymphoma reported in the English literature in the last 10 years from 2000 to 2010 are reviewed.
“…HM of the GYN tract are considered as rare neoplasms; however, there are several cases described in the literature 3,4,6,9,12,13,17,[19][20][21][22][23][24][25][26][27] emphasizing the diagnostic difficulties these tumors pose for the clinician and the pathologist. Although primary HM of GYN is rare, secondary involvement of this anatomical site is reported to be present in 7-30% of women with disseminated disease, 1 or can be seen as a result of relapse of AML 28 or blastic transformation of CML.…”
Section: Discussionmentioning
confidence: 99%
“…Colposcopic findings in primary cervical lymphomas are unremarkable, or if present are rather nonspecific. Diffuse enlargement of the cervix, so-called barrel-shaped cervix or polypoid masses are reported in the literature, 1,4,11,12 whereas ulcerated cervical or vaginal lesions are rarely observed and they tend to be seen in patients with leukemic infiltrates. 13,14 In patients with primary uterine lymphomas, diffuse enlargement of the uterus is often noted, which can mimic fibroids radiologically.…”
The female genital tract is rarely the primary site for hematologic malignancies; however, secondary involvement of this anatomic site is common. Primary lymphomas of the gynecologic tract are reported to represent less than 1% of extranodal non-Hodgkin lymphomas (NHL), and the majority of them being B-cell in origin. Diffuse large B-cell lymphoma is the most common subtype, whereas primary extraosseus plasmacytoma of the genital tract is rare.If clinically not suspected, these rare tumors pose a diagnostic challenge both for clinicians and pathologists. Clinical symptoms are often nonspecific and mimic other more common gynecologic malignancies such as squamous cell carcinoma of the cervix or endometrial adenocarcinoma. Although cervico-vaginal (Pap) smear is the primary screening method for cervical squamous cell carcinoma and its precursors, it is far less sensitive for detection of other primary or metastatic malignancies. In this review, we present three cases of hematologic gynecologic malignancies, two cases of primary NHL, and a case of acute myeloid leukemia with relapse as a pelvic mass, all of which were diagnosed on a liquidbased Pap test. In addition, we discuss the morphologic features of differential diagnostic entities of these rare tumors on conventional and liquid-based preparations.
Background: Primary lymphomas involving the female genital tract are rare, and those arising from cervix are extremely uncommon. They are often misdiagnosed because of their rarity. Methods and cases: The treatment and clinical outcomes of the four cases treated at our institution were compared with the previously published studies. Written informed consent was taken. We highlight four cases of primary diffuse large B-cell lymphoma of cervix treated at our institution with immunochemotherapy and radiotherapy. The mean age was 50 years (range, 39-62 years). Three patients had stage I disease while one had stage II disease. All the patients were in complete remission following treatment with immunochemotherapy and radiation therapy. The average disease free survival was 20 months (range, 8-43 months). None of the patients had any local or systemic relapse. Conclusion: These cases highlight the physicians to be aware of this entity as their management, natural history and prognosis is completely different from squamous carcinomas of the cervix. Surgery should not be attempted in these patients. Immunochemotherapy and radiotherapy results in favorable clinical outcomes.
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