scholarly journals Subungual Nail Erythrasma Presenting as Melanonychia: A Rare Finding

2020 ◽  
pp. 1-5
Author(s):  
Jalal Maghfour ◽  
Jennifer Kane ◽  
Leslie Robinson-Bostom ◽  
John Kawaoka ◽  
Nathaniel Jellinek
Keyword(s):  
Rare Finding

Die Aplasie der Vena cava inferior als Ursache rezidivierender Bein- und Beckenvenenthrombosen

VASA ◽  
1999 ◽  
Vol 28 (4) ◽  
pp. 289-292 ◽  
Author(s):  
Tiesenhausen ◽  
Amann ◽  
Thalhammer ◽  
Aschauer
Keyword(s):  
Inferior Vena Cava ◽  
Inferior Vena ◽  
Heart Defects ◽  
Vena Cava ◽  
Clinical Signs ◽  
Vena Cava Inferior ◽  
Caval Vein ◽  
Rare Finding ◽  
Thrombotic Complications ◽  
Asplenia Syndrome

Congenital anomalies of the caval vein are often associated with other abnormities such as heart defects, situs inversus or a polysplenia-asplenia-syndrome. An isolated, congenital malformation like aplasia of the inferior vena cava is a rare finding. A review of the embryology and abnormities, diagnostics, clinical signs and treatment is given together with the histories of two patients having thrombosis of the lower extremities and pelvic veins, caused by aplasia of the inferior vena cava. After thrombotic complications caused by vena cava aplasia there is high risk of recurrence. Those patients should be anticoagulated for lifetime.

De Garengeot Hernia: Appendicitis within a Femoral Hernia

2005 ◽  
Vol 71 (6) ◽  
pp. 526-527 ◽  
Author(s):  
Gabriel Akopian ◽  
Magdi Alexander
Keyword(s):  
Inguinal Hernia ◽  
Femoral Hernia ◽  
18Th Century ◽  
Hernia Sac ◽  
Rare Finding ◽  
Amyand Hernia ◽  
De Garengeot Hernia

Many surgeons are familiar with Amyand hernia, which is an inguinal hernia sac containing an appendix. However, few surgeons know of the contribution of Rene Jacques Croissant de Garengeot, an 18th century Parisian surgeon, to hernias. He is quoted in the literature as the first to describe the appendix in a femoral hernia sac. We discuss the case of an 81-year-old woman who presented with appendicitis within a femoral hernia, a rare finding at surgery that is almost never diagnosed preoperatively. We also propose crediting Croissant de Garengeot by naming this condition after him. Although his full last name is Croissant de Garengeot, for convenience we suggest the simple diagnosis of “de Garengeot hernia.”

Anteromedial meniscofemoral ligament–A rare finding

Morphologie ◽  
2021 ◽  
Author(s):  
Thaís Amanda Frank de Almeida Alves ◽  
Marco Antonio Alves Braun ◽  
Márcio Luís Duarte ◽  
Lucas Ribeiro dos Santosc
Keyword(s):  
Rare Finding ◽  
Meniscofemoral Ligament

Rare finding of a large parathyroid adenoma with thyroid aplasia

2021 ◽  
Author(s):  
Andriy Hordiychuk ◽  
David S. C. Soon ◽  
Fiona M. Y. Lee
Keyword(s):  
Parathyroid Adenoma ◽  
Rare Finding

scholarly journals Unusual Monteggia type 1 variant in adult: a rare finding in a rare fracture

2018 ◽  
pp. bcr-2018-226789
Author(s):  
Mantu Jain ◽  
Amit Tirpude
Keyword(s):  
Rare Finding

scholarly journals Monochorionic monoamniotic twin pregnancies with two yolk sacs may not be a rare finding: a report of two cases

2010 ◽  
Vol 36 (3) ◽  
pp. 384-386 ◽  
Author(s):  
T. Murakoshi ◽  
K. Ishii ◽  
M. Matsushita ◽  
T. Shinno ◽  
H. Naruse ◽  
...  
Keyword(s):  
Rare Finding ◽  
Twin Pregnancies

Keratin Granulomas in the Peritoneum on Frozen Section: A Case Report with Multiple Suspects and the Search for the Culprit

2021 ◽  
pp. 106689692110160
Author(s):  
Levon Katsakhyan ◽  
Xiaoming Zhang ◽  
Maria C. Reyes ◽  
Lauren E. Schwartz ◽  
Ashley F. Haggerty ◽  
...  
Keyword(s):  
Case Report ◽  
Dermoid Cyst ◽  
Frozen Section ◽  
Endometrioid Adenocarcinoma ◽  
Diagnostic Significance ◽  
Rare Finding ◽  
Fertility Sparing ◽  
Endometrial Endometrioid Adenocarcinoma

Keratin granulomas in the peritoneum are a rare finding with multiple etiologies and can be especially challenging for both the pathologist and the surgeon when these lesions are grossly visible. We report a case of a unique frozen section diagnostic scenario of evaluation of keratin granulomas in the peritoneum of a 47-year-old woman in the setting of multiple potential culprits: endometrial endometrioid adenocarcinoma following fertility sparing treatment, and a concurrent dermoid cyst. We discuss the various etiologies of keratin granulomas in the peritoneum, mechanism of their formation, diagnostic significance, as well as implications of fertility sparing treatments. To the best of our knowledge, this is the only case of keratin granulomas in the peritoneum with multiple distinct potential pathologic culprits as well the only case following fertility sparing treatment.

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