Novel EIF5A-USP6 Gene Fusion in Nodular Fasciitis Associated With Unusual Pathologic Features: A Report of a Case and Review of the Literature

2019 ◽  
Vol 42 (7) ◽  
pp. 539-543 ◽  
Author(s):  
Jiri Lenz ◽  
Michael Michal ◽  
Marian Svajdler ◽  
Nikola Ptakova ◽  
David Lenz ◽  
...  
2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
John E. Riffle ◽  
Andrea H. Prosser ◽  
Jeffery R. Lee ◽  
Julie J. Lynn

Nodular fasciitis is a benign, reactive, fibroblastic proliferation in which nodules most commonly develop in the subcutaneous or superficial fascia of the extremities. The occurrence of these growths in the orbital region is relatively rare. Our intent is to report another orbital case of this benign fibroproliferative tumor and to provide a brief review of the pertinent medical literature. The salient pathologic features of nodular fasciitis are summarized. The potential for the misdiagnosis of these benign mesenchymal tumors as a malignant sarcomatous neoplasm is discussed. It is important for ophthalmologists to be aware of this pathologic entity and its pseudosarcomatous appearance.


2008 ◽  
Vol 49 (10) ◽  
pp. 1999-2002 ◽  
Author(s):  
Preetha Ramalingam ◽  
Asha Nayak-Kapoor ◽  
Michelle Reid-Nicholson ◽  
Jennifer Jones-Crawford ◽  
Celalettin Ustun

2010 ◽  
Vol 134 (12) ◽  
pp. 1785-1792 ◽  
Author(s):  
Artur Zembowicz ◽  
Rajni V. Mandal ◽  
Pitipol Choopong

Abstract Context—Melanocytic proliferations are among the most common neoplasms of the conjunctiva. They often represent challenging lesions for pathologists unfamiliar with unique histologic features of melanocytic proliferations in this location and with nomenclature used by ophthalmologists. Objective—To comprehensively review clinical aspects, pathologic features, and management of melanocytic proliferations of the conjunctiva. Data Sources—Review of the literature and personal experience of the authors. Conclusions—Classification, state of the art, and practical aspects of pathology of melanocytic proliferations of the conjunctiva are discussed.


2021 ◽  
pp. 1-4
Author(s):  
Markus Denzinger ◽  
Markus Denzinger ◽  
Sandra Steininger ◽  
Niels Zorger ◽  
Patricia Reis Wolfertstetter ◽  
...  

Nodular fasciitis is a rare disease, and its diagnosis is difficult. We present a case report of a seven-year-old child with progredient swelling of the left pectoralis muscle three weeks after trauma. After histopathological diagnosis, we performed complete resection. Normally, a conservative approach with regular follow-up is regarded as appropriate since nodular fasciitis does have the capability to regress spontaneously. Since recent publications indicate the possibility of malignant transformation, the complete primary resection also has to be discussed as therapy of choice.


2011 ◽  
Vol 135 (1) ◽  
pp. 143-146 ◽  
Author(s):  
Joshua Anspach Hanson ◽  
Abiy B. Ambaye

Abstract Adult testicular granulosa cell tumors are rare sex cord–stromal tumors of which only 28 have been previously reported. As compared with their ovarian counterparts, these tumors may follow a more aggressive course because the proportion of malignant cases is higher. To date, there are no clinical or pathologic features that definitively predict malignancy. We reviewed all prior case reports for features that may predict their malignant potential. Tumor size greater than 5.0 cm is the only feature statistically associated with malignancy. Mitotic count, tumor necrosis, patient age, and the presence of gynecomastia do not, at present, predict benign versus malignant behavior.


1998 ◽  
Vol 18 (1) ◽  
pp. 1-12 ◽  
Author(s):  
Nobuyuki Kawano ◽  
Saburo Yagishita ◽  
Masamichi Hara ◽  
Mamoru Tadokoro

2013 ◽  
Vol 41 (9) ◽  
pp. 829-833 ◽  
Author(s):  
Wei-Xia Peng ◽  
Mitsuhiro Kudo ◽  
Tetsushi Yamamoto ◽  
Shunta Inai ◽  
Takenori Fujii ◽  
...  

2019 ◽  
Vol 27 (5) ◽  
pp. 535-540
Author(s):  
Cristina Costales ◽  
Arjun Mehta ◽  
Sujit Kulkarni ◽  
Brent K. Larson

The clear cell variant of solid pseudopapillary neoplasm (ccSPN) of the pancreas was first described in 2006. In this article, we report a case of this rare variant and review the few published reports. Both the current and previous reports show that ccSPN has several morphologic differences from conventional SPN, including clear vacuoles, fewer pseudopapillary formations, more solid/diffuse architecture, less hemorrhage, and fewer cholesterol clefts. Some of these features peculiar to ccSPN, such as solid/diffuse architecture, have been proposed to suggest aggressive behavior, though reports of ccSPN are rare and often have limited clinical follow-up. ccSPN also appears to occur more frequently in males than conventional SPNs. These clinical and pathologic features lead to unique set of differential diagnostic considerations for ccSPN, including metastatic renal cell carcinoma, perivascular epithelial cell tumor, and clear cell variants of other carcinomas. These unique features, atypical differential, and uncertain prognostic ramifications all make ccSPN an important variant to be aware of and report.


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