Citations

Citations to this article as recorded by  

• Primary and metastatic squamous cell carcinoma of the thyroid gland: Two case reports
  Xing Zhao, Pengyu Hao, Jiangbei Tian, Jirun Sun, Dawei Chen, Zhehui Cui, Libo Xin, Yanmin Song, Gang Zhang
  Open Life Sciences.2022; 17(1): 1148.     CrossRef
• Aggressive Thyroid Gland Carcinoma: A Case Series
  JP Dworkin-Valenti
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Orbital solitary fibrous tumor (SFT) has recently been proposed as the encompassing terminology for hemangiopericytoma, giant cell angiofibroma (GCAF), and fibrous histiocytoma of the orbit. The lacrimal gland is a very rare location for both SFT and GCAF. A 39-year-old man presented with a painless left upper eyelid mass. An orbital computed tomography scan identified a 1.1 cm-sized well-defined nodule located in the left lacrimal gland. He underwent a mass excision. Histopathologic examination showed a proliferation of relatively uniform spindle cells with a patternless or focally storiform pattern. Dilated vessels were prominent, but angiectoid spaces lined with giant cells were absent. Floret-type giant cells were mostly scattered in the periphery. The tumor was immunoreactive for CD34 and CD99, but negative for smooth muscle actin and S-100 protein. This is the first Korean case of SFT of the lacrimal gland with overlapping features of GCAF, suggesting a close relationship between the two entities.

Citations

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• A review of solitary fibrous tumours of the orbit and ocular adnexa
  Cornelius René, Paolo Scollo, Dominic O’Donovan
  Eye.2023; 37(5): 858.     CrossRef
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• Giant cell-rich solitary fibrous tumour of the lacrimal gland with prominent angiomatoid cystic changes and an underlying NAB2ex3-STAT6ex18 fusion
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• Cystic appearance - a new feature of solid fibrous tumours in the lacrimal gland: a case report with literature review
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• Solitary Fibrous Tumor in the Lacrimal Gland Fossa: A Case Report
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• Ocular adnexal (orbital) solitary fibrous tumor: nuclear STAT6 expression and literature review
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• Angiofibroma de células gigantes en mucosa yugal: una entidad rara en una localización infrecuente
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We describe a rare case of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) associated with a six-year history of autoimmune pancreatitis, which was controlled by steroid treatment. The patient presented with multiple, cervical and thoracic lymphadenopathy and abnormal, nodular opacities in the lung. Histologically, Rosai-Dorfman disease with numerous IgG4-positive cells was identified in a subcutaneous lymph node in the patient's left forearm. The patient recovered uneventfully with steroid treatment.

Citations

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• Lung Involvement in Destombes-Rosai-Dorfman Disease
  Quentin Moyon, Samia Boussouar, Philippe Maksud, Jean-François Emile, Frédéric Charlotte, Nathalie Aladjidi, Grégoire Prévot, Jean Donadieu, Zahir Amoura, Philippe Grenier, Julien Haroche, Fleur Cohen Aubart
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• Rosai-Dorfman Disease: Rare Pulmonary Involvement Mimicking Pulmonary Langerhans Cell Histiocytosis and Review of the Literature
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• A subset of Rosai–Dorfman disease cases show increased IgG4‐positive plasma cells: another red herring or a true association with IgG4‐related disease?
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