scholarly journals Superficial myofibroblastoma of the vagina with a stalk: case report of a rare vaginal tumor with notable radiological findings

2021 ◽  
Vol 16 (12) ◽  
pp. 3690-3694
Author(s):  
Yui Tomita ◽  
Eriko Takabayashi ◽  
Sayaka Yuzawa ◽  
Atsutaka Okizaki
2020 ◽  
Vol 11 (1) ◽  
pp. 21
Author(s):  
Claudia Brogna ◽  
Valentina Milano ◽  
Barbara Brogna ◽  
Lara Cristiano ◽  
Giuseppe Rovere ◽  
...  

The partial trisomy 13q encompasses an extensive variability of phenotypic and radiological findings including leukoencephalopathy and brain malformations such as holoprosencephaly, callosal dysgenesis, hippocampal hypoplasia, olfactory hypoplasia, and vermian hypoplasia. We report for the first time a case of a 23-year-old patient affected by de novo partial 13q22.1q34 trisomy (41.7 Mb, 72,365,975-114,077,122x3) presenting with hemiparesis related to both ischemic and haemorrhagic cerebral lesions compatible with cerebral vasculitis due to a possible combination of genetic and immunological interaction.


2015 ◽  
pp. 20150057
Author(s):  
A Abdullah ◽  
P Entezami ◽  
L Halpin ◽  
J Feldmeier ◽  
R E Mrak ◽  
...  

2004 ◽  
Vol 50 (2) ◽  
pp. 139
Author(s):  
Sung Keun Park ◽  
Seok Jin Choi ◽  
Auh Whan Park ◽  
Yong Woo Kim ◽  
Hae Woong Jeong ◽  
...  

Author(s):  
Banu Yigit ◽  
Mert Tanal ◽  
Bulent Citgez

Abstract Brown tumor (BT) is the pathological expression of osteitis fibrosa cystica owing to primary and secondary hyperparathyroidism (HPT). It is a rare benign lesion of skeletal system that usually affects the facial bones, clavicles, ribs, pelvis and extremities. The purpose of this case report is to present the clinical, pathological and radiological findings of BT, rarely seen in adults, originating from the giant parathyroid adenoma and emerging as the first clinical sign of HPT. The patient underwent a successful parathyroidectomy operation and on the first postoperative day, the patient was discharged without any complications. Continuous...


2019 ◽  
Vol 12 ◽  
pp. 117954761984383
Author(s):  
Siu W Lam ◽  
Philip VM Linsen ◽  
Otto E Elgersma

The urachus is a vestigial structure of the allantois and cloaca. It involutes as fetal development progresses to become a fibrous cord, which courses between the umbilicus and bladder dome within the retropubic space. Infection occasionally occurs in patients with congenital patent urachus. Here, we report a patient with infection of a previously closed urachal tract presenting as an abdominal mass. This has rarely been described in the literature. Current knowledge on imaging findings to the diagnosis is discussed.


2020 ◽  
Vol 6 (2) ◽  
pp. 20190127
Author(s):  
Kino Ceon Francis ◽  
Candice Daley ◽  
Bonnie-Paul Regis Williams ◽  
Richard Bullock ◽  
Ulanda Singh ◽  
...  

The transmesosigmoid hernia is a rare type of sigmoid mesocolon hernia. Its presentation is non-specific and thus hardly ever preoperatively diagnosed. Its diagnosis often requires surgical corroboration. This case report aims to improve on the preoperative diagnosis with a proposed observed sign on CT. All literature reviewed described radiological findings related to the small bowel; thus, features of small bowel obstruction was the “hallmark” of internal hernias. This paper intends to describe the features of the sigmoid mesocolon internal hernias, illustrate and propose a never reported configuration of the sigmoid colon. This sigmoid colon configuration has a resemblance to the omega sign. We intend to present a new hallmark sign, which may serve as a clue in the identification of internal hernias involving the sigmoid mesocolon.


2019 ◽  
Vol 2019 (11) ◽  
Author(s):  
Narendra Pandit ◽  
Tek Narayan Yadav ◽  
Deepa Shrestha ◽  
Purbesh Adhikari ◽  
Laligen Awale

Abstract Inflammatory myofibroblastic tumor (IMFT) of the colon is a very rare entity, characterized by proliferation of myofibroblast cells admixed with inflammatory infiltrates. The entity was first described in the late 1990s, and since then less than 30 cases have been described. It frequently mimics other neoplasm of the colon, such as adenocarcinoma, lymphoma and stromal tumor, and is very difficult to clinch the diagnosis preoperatively based on the clinical and radiological findings. Here, we discuss an uncommon case of sigmoid IMFT in a 35-year old male, presenting with bleeding per rectum and managed successfully by colectomy.


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