Orbital Reticulum-cell Sarcoma: Report of Nine Cases.
نویسنده
چکیده
RETICULUM-CELL sarcomata, together with leukaemia, Hodgkin's disease, giant follicular lymphoblastoma (Brill Symmer's disease), lymphosarcoma, and lymphoma, constitutes a group of lymphomatous or reticular tumours. These different lymphoblastomata appear to represent pleomorphism of the reticular system to unknown causal stimuli (Ginsburg, 1934; Gall and Mallory, 1942; Herbut, Miller, and Erf, 1945). The nomenclature of these tumours in the literature is confused, and identical lesions have been described by various writers as lymphomata, lymphoblastomata, lymphocytomata, malignant lymphomata, lymphosarcomata, reticular-cell type of lymphosarcomata, reticulo-sarcomata, and round-cell sarcomata. DukeElder (1952) states that: "reticulosarcoma of the orbit is not commonly noted in the literature, but it is probable that several cases have been described as lymphosarcomata. Its occasional occurrence is, however, undoubted (Wilson, 1940; McGavic, 1943)." Histological differentiation between lymphoid tumours and reticulum-cell tumours is often difficult, and both cell elements may participate in the formation of the same tumour (Pfanz, 1957). The histological structure may change in the course of the disease when a previously benign tumour becomes malignant. However, the various types of lymphomatous tumours may be differentiated by their clinical behaviour and by the nature of the cells and intercellular fibres constituting the tumour. Lymphomata are benign tumours composed of differentiated lymphocytes, but lymphosarcomata are highly invasive tumours. Their component cells are similar to lymphocytes, consisting of a mere rim of faintly stained cytoplasm and a relatively large nucleus with a dense chromatin network. The cells are closely and uniformly packed. Numerous mitotic figures are present. Lymphomata and lymphosarcomata may both be associated with leukaemia. Giant follicular lymphadenopathy is essentially a lymphocytic hyperplasia and may arise from several different causes. Reticulosarcoma cells are fairly large, and of varied shapes, round, polyhedral, oval, or irregular. Their cytoplasm is feebly stained, with a relatively
منابع مشابه
Ostegogenic Sarcoma with Epithelial Differentiation (Carcinosarcoma): Report of Two Cases
Epitheloid osteosarcoma (carcinosarcoma) of the bone is a rare malignant tumor and only a few cases have been reported in the literature. In this study, we report two cases of osseous carcinosarcoma (epitheloid osteosarcoma) with immunohistochemical studies. The morphological and immunohistochemical data in these two cases support the theory of divergent differentiation of primitive, uncommitt...
متن کاملClear cell sarcoma of the hand: a case of malignant melanoma of soft parts
A case is reported with clear cell sarcoma (CCS) of the hand. Early diagnosis of clear cell sarcoma is always difficult due to its slow growing nature, benign clinical appearance, lack of pigmentation in most cases, and relatively young age of patients which make it to clinically appear as a benign soft tissue tumor. We report a case of clear cell sarcoma of hand in a 56 year old male with a no...
متن کاملDIAGNOSIS OF PRIMARY CARDIAC TUMORS: REPORT OF 30 CASES
Between I 9H I and 1993,30 cases of primary cardiac tumors were diagnosed at the Imam Khomeini Hospital. 20 patients were female and 10 were male, with an average age of 32 years (ranging from 17 days to 65 years of age). The mean duration of symptoms before diagnosis was 6 months, with dyspnea and palpitation being the most common symptoms (60%) and cardiac' murmurs the most usual signs (...
متن کامل[Orbital lymphomas. Presentation of nine cases].
PURPOSE To report nine cases of orbital lymphomas. METHODS We reviewed the clinical records of nine patients diagnosed with orbital lymphoma and performed a literature search related to this condition. RESULTS We present a series of five women and four males with orbital lymphoma involving the orbital region. In our cases, most patients presented concurrent extraorbital lymphoma when the or...
متن کاملPrimary Synovial Sarcoma Presenting as a Huge Mass: A Report of a Rare Case and Review of Literature
Primary synovial sarcoma of mediastinum is very rare among soft tissue sarcomas. Only a few cases have been reportedin the literatures. The best treatment is still unclear, but, surgical resection is the main therapy. In this article we reporta case of a 20*20 cm (2000gr) primary giant mediastinal synovial sarcoma in a 42 year-old man. We performed radicalexcision of the tumor...
متن کاملSynovial Sarcoma-A Rare Tumor of the Larynx
Introduction: Malignant mesenchymal tumors of the larynx are rare. One type of malignant mesenchymal tumor is synovial sarcoma with unknown histogenesis, which occurs predominantly in the lower extremities of young adults. The head and neck region is a relatively rare location. There are few cases of malignant mesenchymal tumors with laryngeal localization in literature. Case Report: In this r...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The British journal of ophthalmology
دوره 45 5 شماره
صفحات -
تاریخ انتشار 1961