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1.
World Neurosurg ; 106: 1053.e1-1053.e5, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28711535

ABSTRACT

BACKGROUND: Primary central nervous system (CNS) histiocytic sarcoma is an extremely rare lymphoproliferative disorder that affects the CNS and behaves aggressively. Only 27 cases of primary CNS histiocytic sarcoma have been reported. The paucity of literature on this entity has made diagnosis and treatment difficult both for the surgeon and the pathologist. CASE DESCRIPTION: In this case of primary CNS histiocytic sarcoma, a middle-aged woman presented from an outside institution with a supposed cerebellar abscess. Intraoperative frozen pathology was initially interpreted as high-grade glioma; however, final pathology demonstrated histiocytic sarcoma. CONCLUSIONS: This report makes a significant contribution to the literature on this rare malignant disease by outlining a similar presentation among several cases and providing a thorough overview of existing criteria for diagnosis and management.


Subject(s)
Brain Abscess/surgery , Brain Neoplasms/surgery , Glioma/surgery , Histiocytic Sarcoma/surgery , Sarcoma/surgery , Brain Abscess/diagnosis , Brain Abscess/etiology , Brain Neoplasms/complications , Brain Neoplasms/diagnosis , Brain Neoplasms/pathology , Diagnosis, Differential , Female , Glioma/diagnosis , Histiocytic Sarcoma/diagnosis , Humans , Meningitis/diagnosis , Middle Aged , Sarcoma/diagnosis
2.
Rare Tumors ; 8(4): 6657, 2016 Nov 17.
Article in English | MEDLINE | ID: mdl-28191295

ABSTRACT

Prostate cancer is the most common malignancy of men in the United States. Small-cell carcinoma (SCC), which typically presents as an aggressive lung malignancy, is a rare diagnosis within the setting of prostate cancer pathology. Due to its limited prevalence, little information regarding the treatment and prognosis of this disease in large populations is available. To date our current knowledge base is largely limited to case reports and retrospective case reviews. The mainstay of treatment for this particular histology most often involves a multimodality approach utilizing chemotherapy in conjunction with radiation therapy, androgen deprivation therapy, or prostatectomy. Here we present the case of an elderly 89-year-old Caucasian male who was diagnosed with SCC of the prostate. Despite proceeding with a course of definitive radiotherapy, the patient experienced rapid progression of disease and ultimately elected to discontinue radiation therapy and receive hospice care.

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