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1.
Int J Gynecol Pathol ; 32(5): 471-5, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23896707

ABSTRACT

Through this case presentation and a review of the literature, we aim to describe clinical and pathologic features and to distinguish the outcome of these tumors. A 25-year-old woman presented with pelvic pain and an iliac mass. Workup revealed a 53-mm cystic partitioned mass of the left ovary infiltrating the left sacrum. She underwent a left adnexectomy. Gross examination revealed a ruptured ovarian mass. When dissected, it showed grayish cerebroid aspects. Histologic examination revealed a malignant tumor proliferation of the diffuse large cells. An immunohistochemical analysis showed negative results for PLAP, αFP, ßHCG, CD117, CK20, and CD30. It also showed lack of B markers and T marker (CD3) and an expression of CD138 and anaplastic lymphoma kinase. The patient was treated by 6 cycles of CHOP chemotherapy and a pelvic radiotherapy. She presented with a 15-cm splenomegaly 26 months later and died of febrile neutropenia. Most patients follow an aggressive disease and are unlikely to respond to the standard.


Subject(s)
Biomarkers, Tumor/metabolism , Lymphoma, B-Cell/pathology , Lymphoma, Large B-Cell, Diffuse/pathology , Receptor Protein-Tyrosine Kinases/metabolism , Adult , Anaplastic Lymphoma Kinase , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Cell Differentiation , Cyclophosphamide/administration & dosage , Diagnosis, Differential , Doxorubicin/administration & dosage , Fatal Outcome , Female , Humans , Immunohistochemistry , Lymphoma, Large B-Cell, Diffuse/drug therapy , Lymphoma, Large B-Cell, Diffuse/surgery , Prednisone/administration & dosage , Vincristine/administration & dosage
3.
Ann Pathol ; 27(3): 247-50, 2007 Jun.
Article in French | MEDLINE | ID: mdl-17978701

ABSTRACT

Inflammatory pseudotumor (IPT) of the spleen is an uncommon entity with debated etiology, characterized by a mixture of inflammatory cells and a component of myofibroblastic spindle cells. This lesion needs to be distinguished from the follicular dendritic cell tumor and the inflammatory myofibroblastic tumor. We report two cases of splenic PTI in a 69-year old and a 62-year old women. The tumors measured respectively 80 and 30 mn in greatest dimension. An inflammatory pseudotumor was histopathologically diagnosed following a splenectomy.


Subject(s)
Granuloma, Plasma Cell/pathology , Inflammation/pathology , Splenic Neoplasms/pathology , Aged , Female , Granuloma, Plasma Cell/surgery , Humans , Middle Aged , Splenic Neoplasms/surgery
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