Chondroid lipoma associated with osteoclast-like multinucleated giant cells - a case report

Apmis ◽  
2017 ◽  
Vol 125 (5) ◽  
pp. 506-508 ◽  
Author(s):  
Mohammed Alyousef ◽  
Areej Al Nemer
2021 ◽  
Vol 6 (2) ◽  
pp. 155-158
Author(s):  
Rohini Sebastian ◽  
Meethu Rappai

Central giant cell granuloma is a reparative bony lesion characterised by abundant multinucleated giant cells within a sea of spindle shaped mesenchymal stromal cells. Giant cells are scattered throughout the fibrovascular connective tissue stroma containing hemorrhage. Its coexistence with parathyroid adenoma is very rare. Brown tumour is a close differential in this scenario. Herein we present the case of a central giant cell granuloma of maxilla and parathyroid adenoma diagnosed almost during the same time in a 58 years old male.


2012 ◽  
Vol 8 (3) ◽  
Author(s):  
Shelly Arora ◽  
Aadithya B. Urs ◽  
Jeyaseelan Augustine ◽  
Priya Kumar ◽  
Ashi Singh

Introduction: Cherubism is a rare, non-neoplastic, self-limiting, fibro-osseous disease, characterized by painless expansion of the maxilla, mandible or both. It usually develops in the first and second year of life. The radiographic appearance presentation is ordinarily bilateral, multilocular appearance in the mandible. To the best of our knowledge, very few cases (less than ten) of non-familial cherubism have been reported in the English literature. Objective: To describe non-familial case of cherubism in a 10-year-old child. Materials and methods: The current case was clinically, radiographically and histopathologically analysed for confirmatory diagnosis. Results: H & E stained section showed vascular and cellular stroma containing numerous multinucleated giant cells. Conclusion: Correlating radiographically and histopathologically the case was finally diagnosed as non-familial variant of cherubism.


Author(s):  
Keval A. Patel ◽  
Kinalee P. Chothani ◽  
Bimal Patel ◽  
Dhaneshwar N. Lanjewar

Xanthogranulomatous inflammation of ovary is a rare disease that is characterized by presence of large number of lipid laden macrophages with an admixture of neutrophils, lymphocytes, plasma cells and multinucleated giant cells. It is misdiagnosed as ovarian tumour that leads to extensive surgery including hysterectomy. In this report we describe a case of Xanthogranulomatous salpingo-oophoritis along with review of literature.


1977 ◽  
Vol 63 (4) ◽  
pp. 387-396 ◽  
Author(s):  
Luciano Lombardi ◽  
Silvana Pilotti ◽  
Antonino Carbone ◽  
Franco Rilke

A soft tissue malignant fibrous histiocytoma was studied by light and electron microscopy. The presence of fibroblast-like cells, histiocyte-like cells, undifferentiated stem cells, and xanthomatous cells was confirmed. Fibroblast- and histiocyte-like multinucleated giant cells were also observed. The observation of lysosomes in some fibroblast-like cells, the features of undifferentiated stem cells, and the presence of cells with intermediate characteristics common to xanthomatous, histiocytic, and stem cells suggest a strict relationship among these cellular types.


BMC Cancer ◽  
2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Vincenzo Fiorentino ◽  
Francesco Pierconti ◽  
Niccolò Lenci ◽  
Martina Calicchia ◽  
Giuseppe Palermo ◽  
...  

1991 ◽  
Vol 30 (6) ◽  
pp. 1109-1114
Author(s):  
Yuji HINOURA ◽  
Kousuke MARUTSUKA ◽  
Tohru HAYASHI ◽  
Yatsuki ARATAKE ◽  
Sachiya OHTAKI ◽  
...  

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