scholarly journals A rare presentation: A case report of osseous metaplasia and mature bone formation in a follicular adenoma of the thyroid

2017 ◽  
Vol 37 ◽  
pp. 83-86
Author(s):  
Nadia Aurora ◽  
Insia Hashmi ◽  
Subhasis Misra ◽  
Nail Aydin
2017 ◽  
Vol 5 ◽  
pp. 2050313X1774631 ◽  
Author(s):  
Haneen Al-Maghrabi ◽  
Abdelrazak Meliti

Gastrointestinal stromal tumors are the most common primary mesenchymal tumors of the gastrointestinal tract accounting for 0.1%–3.0% of all gastrointestinal malignancies. The stomach is the most common site (60%) followed by the small bowel (30%–35%) particularly jejunum and ileum, colorectum (5%) and rarely affect esophagus and appendix. Most gastrointestinal stromal tumors arise sporadically, however, less commonly they develop in association with various clinical syndromes like Carney triad, Carney–Stratakis syndrome, familial gastrointestinal stromal tumor syndrome and neurofibromatosis type1 (NF1). We report a 65-year-old male patient presented with gastric mass (7.5 × 4.5 × 3.5 cm) arising from the posterior gastric wall. Histologic examination revealed neoplastic proliferation of spindled and epithelioid cells with focal plexiform pattern and low mitotic activity 3/50 HPF. No evidence of cytological atypia, abnormal mitosis or necrosis. Interestingly enough, there were focal areas of mature bone formation/osseous differentiation associated with calcification. The tumor cells were strongly positive for CD117, DOG1 with focal immunoreactivity against CD34. The morphologic features and the immunoprofile were diagnostic of gastrointestinal stromal tumor. Herein, we present a rare case of gastric gastrointestinal stromal tumor with mature bone formation, osseous metaplasia and calcification. To the best of our knowledge, this is the second case report of gastric gastrointestinal stromal tumor with osseous differentiation and mature bone formation.


2013 ◽  
Vol 03 (04) ◽  
pp. 137-138
Author(s):  
Harish S. Permi

AbstractOsseous metaplasia is a rare histologic feature associated with renal cell carcinoma, occurring in a contracted kidney is still rarer. Metaplastic bone formation within the renal tumor gives an appearance similar to that of calcification. It is difficult to distinguish between bone formation and calcification on the basis of radiological imaging alone. Prognostic significance of metaplastic bone formation in renal cell carcinoma is not clear, however some report suggest good prognosis as a result of limitation of tumor spread by bone formation. This case report highlights the occurrence of renal cell carcinoma with osseous metaplasia in a contracted kidney.


2013 ◽  
Vol 6 (4) ◽  
pp. 977-979 ◽  
Author(s):  
JI-SUN CHUN ◽  
RAN HONG ◽  
JUNG-A KIM

Author(s):  
Dr. Amol N Wagh ◽  
◽  
Dr. Samprathi D ◽  
Dr. Shirish R Bhagvat ◽  
Dr. Amarjeet Tandur ◽  
...  

Anaplastic thyroid cancer is the most advanced and aggressive thyroid cancer. It is very rare and isfound in less than 2% of patients with thyroid cancer. It most commonly occurs in people over theage of 60 years. It is usually diagnosed at later stages when the disease has already spread tosurrounding structures or has grown large enough to compress the trachea or esophagus causingpressure symptoms. The patient here, a 75-year-old female, presented with a large swelling in thefront of the neck in euthyroid status which was diagnosed as anaplastic thyroid cancer and wasmanaged surgically and the surgical specimen was sent for histopathological examination. Thepresence of osseous metaplasia with mature bone formation in anaplastic thyroid carcinoma is a rareentity and has been discussed in this case report.


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