Usefulness of a diagnostic algorithm hyperferritinemia: A case report of a Spanish family with hereditary hemochromatosis and mutation in SLC40A1 gene

2015 ◽  
Vol 145 (1) ◽  
pp. 42-43
Author(s):  
Juan Antonio Vargas ◽  
Alejandro Muñoz ◽  
Begoña Samper ◽  
Belén Bornstein
Medicine ◽  
2019 ◽  
Vol 98 (44) ◽  
pp. e17526
Author(s):  
Xin Yin ◽  
Yu Zhang ◽  
Hui Gao ◽  
Qing-long Jin ◽  
Xiao-yu Wen

Diabetes Care ◽  
2006 ◽  
Vol 29 (2) ◽  
pp. 464-466 ◽  
Author(s):  
J.-U. Hahn ◽  
M. Steiner ◽  
S. Bochnig ◽  
H. Schmidt ◽  
P. Schuff-Werner ◽  
...  

2009 ◽  
Vol 47 (3) ◽  
pp. 219-222 ◽  
Author(s):  
Ketil Thorstensen ◽  
Kjartan Egeberg ◽  
Inge Romslo ◽  
Jørn Dalhøj ◽  
Preben Wiggers

2010 ◽  
Vol 48 (3) ◽  
pp. 518-527 ◽  
Author(s):  
Vincent C. Marconi ◽  
Richard Kradin ◽  
Francisco M. Marty ◽  
Duane R. Hospenthal ◽  
Camille N. Kotton

1999 ◽  
Vol 195 (7) ◽  
pp. 509-513 ◽  
Author(s):  
Heinz-Hermann Köhler ◽  
Thomas Höhler ◽  
Ulla Küsel ◽  
Charles James Kirkpatrick ◽  
Peter Schirmacher

2011 ◽  
Vol 2011 (jan20 1) ◽  
pp. bcr0720103151-bcr0720103151 ◽  
Author(s):  
M. Colotto ◽  
M. Maranghi ◽  
A. Epifania ◽  
M. Totaro ◽  
R. Giura ◽  
...  

Open Medicine ◽  
2021 ◽  
Vol 16 (1) ◽  
pp. 899-903
Author(s):  
Ljiljana Vučković ◽  
Aleksandra Klisic ◽  
Mirjana Miladinović

Abstract Background During embryonic development in women, a regression of temporary embryonic structures – mesonephric (Wolffian) ducts occurs. Adnexal tumors of Wolffian duct origin (FATWO) are rare. Case report We presented the case of a 64-year-old female patient who was diagnosed with FATWO. After the surgical treatment, the uterus with bilateral adnexal structures was submitted for histopathological analysis. The left ovary was occupied by a tumor measuring 80 × 60 × 50 mm, with smooth, shiny, whitish surface. Tumor cells were medium-sized, relatively uniform, round, and polygonal, with eosinophilic cytoplasm and centrally laid nucleus with fine chromatin, organized into solid, trabecular, and tubular formations. Tumor cells were positive for pancytokeratin (CK), CK7, CD10, neuron-specific enolase (NSE), synaptophysin, calretinin, progesterone, estrogen, and epithelial membrane antigen (EMA). Conclusion This case adds a report of a rare tumor to the literature. We must think of it in the differential diagnostic algorithm to make an accurate diagnosis for selecting the best treatment modality.


Sign in / Sign up

Export Citation Format

Share Document