Giant-Cell Lesion in a Sesamoid Bone of the Thumb

1998 ◽  
Vol 23 (2) ◽  
pp. 279-280 ◽  
Author(s):  
E. P. CLARKE ◽  
J. W. PRITCHETT

We treated a 72-year-old woman by excision of the right thumb sesamoid which contained a giant-cell lesion. Nine years later she had normal function and no evidence of other lesions, recurrence or metastasis. We recommend that the diagnosis of giant-cell reparative granuloma and giant-cell tumour be considered when a bony mass in a sesamoid bone is discovered. Surgical excision at least in our one case was definitive treatment.

Hand Surgery ◽  
2005 ◽  
Vol 10 (01) ◽  
pp. 97-100 ◽  
Author(s):  
Narayan Hulse ◽  
Stewart J. Watson

Giant cell tumour of the tendon sheath is uncommon in children. We describe this tumour arising from the right ring finger in an eight-year-old girl. Plane radiographs showed a soft tissue mass with erosion of the distal phalanx. The tumour was treated by surgical excision with good outcome.


2018 ◽  
pp. bcr-2018-225095
Author(s):  
Duarte Rosa ◽  
Raquel Baptista Dias ◽  
João Cunha Salvador ◽  
Alexandra Borges

We report the case of a 74-year-old man with a giant cell tumour (GCT) of the right maxilla and pterygoid process. The patient presented to the maxillofacial and head and neck surgery clinic with an ulcerated lesion of the hard palate. Initial workup with CT revealed a mass within the right maxillary sinus and pterygoid process with associated bone expansion and erosion. Biopsy showed a GCT with mucosal ulceration. Two years after surgical resection, a follow-up CT revealed tumour recurrence involving the right pterygoid process and lateral pterygoid muscle. The patient was then proposed for therapy with denosumab. Under denosumab treatment, the lesion maintained stable dimensions and became sclerotic and heavily ossified.


2006 ◽  
Vol 126 (7) ◽  
pp. 779-781 ◽  
Author(s):  
Gino Marioni ◽  
Rosario Marchese-Ragona ◽  
Luca Guarda-Nardini ◽  
Roberto Stramare ◽  
Elia Tognazza ◽  
...  

2021 ◽  
Vol 2021 ◽  
pp. 1-7
Author(s):  
Álvaro Bengoa-González ◽  
Enrique Mencía-Gutiérrez ◽  
Beatriz Alonso-Martín ◽  
Bianca-Maria Laslău ◽  
Elena Salvador ◽  
...  

Giant cell reparative granuloma (GCRG) is a rare fibroosseous lesion uncommonly seen in the orbital area. Although benign, it is known to be recurrent and locally destructive. We report two cases of GCRG of the orbit. In both cases, computed tomography revealed a heterogeneously growing well-defined mass, arising from the roof of the orbit, affecting the cortex, and invading the orbit. In the first case, the mass extended into the anterior cranial fossa. Magnetic resonance imaging with gadolinium showed, in both cases, a cystic character of the lesion with fluid levels. The surgical treatment was performed via an upper crease incision. An ultrasonic aspirator system was used to remove the tumor tissue and its extension into cranial fossa. Careful histopathologic analysis established the diagnosis of GCRG. Symptoms resolved completely with no evidence of recurrence after a follow-up of 18 and 14 months, respectively. We present the clinicopathological and radiological findings, and we describe the surgical approach. As a rare entity, GCRG of the orbit should be considered in differential diagnosis of fibroosseous orbital masses. Complete surgical excision carries a low risk of recurrence.


2021 ◽  
Vol 07 (1&2) ◽  
pp. 1-3
Author(s):  
Sampa Choudhury ◽  

Giant Cell Reparative Granuloma (GCRG) is an unusual non-neoplastic lesion which most commonly involves maxilla and mandible. We present a case of GCRG of the nasal cavity in a young female presented with the complaint of progressively nasal obstruction. Radiological findings are usually nonspecific in this entity, therefore a good clinical, radiological and pathological correlation is needed for final diagnosis and to differentiate it from other giant cell lesions. Surgical excision is the preferred treatment modality over simple curettage.


2012 ◽  
Vol 27 (2) ◽  
pp. 24-27 ◽  
Author(s):  
Somnath Saha ◽  
Sharmila Sen ◽  
V. Padmini Saha ◽  
Sudipta Pal

Objective: To present a rare case of maxillary swelling; its investigation and management.   Methods: Design: Case Report   Setting: Tertiary Rural Private Teaching Hospital   Patient: One   Results: A 45-year-old female presented with a right maxillary swelling of six months duration. Radiological investigation revealed a radiolucent lesion arising from the inferior aspect of the right maxilla with no areas of calcification. Incisional biopsy report was consistent with giant cell tumor. The mass was excised via a Weber Ferguson incision under general anesthesia. Conclusion: Though rare, giant cell tumor should be considered as one of the differential diagnosis in cases of maxillary swelling. Adequate surgical excision with long-term follow-up should be the treatment of choice for managing a giant cell lesion of the maxilla.   Keywords: maxillary swelling, giant cell tumor


1995 ◽  
Vol 109 (6) ◽  
pp. 538-541 ◽  
Author(s):  
W. G. McCluggage ◽  
G. B. McBride ◽  
W. J. Primrose ◽  
J. Cullan ◽  
E. J. McNaboe ◽  
...  

AbstractWe report a case of giant cell tumour of the temporal bone arising in a 31-year-old man. The presenting symptoms were unusual, being rotational vertigo, unilateral tinnitus, and hearing loss. A computed tomography (CT) scan showed a large mass within the right temporal bone and the infratemporal fossa. The radiological appearance was suggestive of an aggressive primary neoplasm arising within bone. Biopsy and subsequent resection showed a giant cell tumour of bone. The tumour was histological grade 1. At two-year follow-up, there was no evidence of tumour recurrence or metastasis.


2019 ◽  
Vol 99 (1) ◽  
pp. 39-41
Author(s):  
Drake Mc Arthur, MD ◽  
Enrique Palacios ◽  
Jeremy Nguyen

A case of a 32-year-old female with a known diagnosis of Turner syndrome who presented with complaints of chronic progressive right-sided facial pain and sinus pressure and who was afebrile. On physical examination, there was eye proptosis on the right and significant increased fullness in the right infraorbital and maxillary regions. Computed tomography and magnetic resonance imaging demonstrated a large expansile space-occupying lesion in the right maxillary area that histologically turned out to be a giant cell reparative granuloma. The lesion was completely removed, and of interest, the patient was followed up both clinically and on imaging for 10 years with no signs of recurrence. A discussion on this entity, as well the clinical and imaging differential diagnoses, is discussed.


2021 ◽  
Author(s):  
Jiannan Li ◽  
Weizhong Zhang ◽  
Guangzhi Wu ◽  
zhan zhang

Abstract Background: Giant cell lesion of small bones (GCLSB), also known as giant cell reparative granuloma, is a rare tumor-like condition occurring in the small bones of the hands and feet. GCLSB lacks specific clinical, radiological, and histological manifestations. There are no standardized protocols for treatment. Case presentation: Here, we report a 16-year-old male with recurrent GCLSB in the proximal phalanx of the left thumb. The lesion was successfully resected with bone grafting. Conclusions: We summarized the characteristics of 33 reported cases of GCLSB from 1983 to date, including gender, age, lesion sites, recurrence, and treatment. We conclude that resection and reconstruction with curettage is the treatment of choice.


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