scholarly journals Combined Fundal and Segmental Adenomyomatosis of the Gallbladder in a Child: A Rare Case Report

2019 ◽  
Vol 2019 ◽  
pp. 1-4
Author(s):  
Hidetoshi Kinoshita ◽  
Hiromichi Ariga ◽  
Jun Shirota ◽  
Kyosuke Sasaki ◽  
Yasuko Shibukawa ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Rare Case ◽  
Correct Diagnosis ◽  
Muscle Layer ◽  
Solid Mass ◽  
Mucosal Hyperplasia ◽  
Rare Case Report ◽  
Initial Imaging

Adenomyomatosis of the gallbladder (AMG) is characterized by mucosal hyperplasia leading to invagination through the thickened muscle layer, which is relatively common in adults, but is rare in childhood. We report a 12-year-old boy with adenomyomatosis of the gallbladder combined segmental and fundal type. This combined type is rare in adults and is first reported here in childhood. Although initial imaging with computed tomography (CT) suggested the presence of a circular solid mass-like lesion because of its rare morphology, repeated ultrasonography (US) was useful for leading to a correct diagnosis.

scholarly journals Primary pulmonary meningioma mimicking pulmonary metastasis: A rare case report

2020 ◽  
Vol 28 (4) ◽  
pp. 699-701
Author(s):  
Nesrin Gürçay
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Pulmonary Metastasis ◽  
Pulmonary Nodule ◽  
Chest Radiography ◽  
Rare Case ◽  
Benign Tumors ◽  
Female Case ◽  
Rare Case Report

Primary pulmonary meningiomas are rare and mostly benign tumors. They usually appear as a solid peripheral pulmonary nodule on chest radiography and computed tomography and are frequently diagnosed incidentally. Herein, we report a 55-year-old female case of primary pulmonary meningioma mimicking pulmonary metastasis.

scholarly journals A RARE CASE REPORT OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT

2021 ◽  
Vol 71 (2) ◽  
pp. 724-26
Author(s):  
Mussadique Ali ◽  
Chandumal . ◽  
Manzoor Khan ◽  
Jhanzeb Iftikhar ◽  
Samia Yasmeen ◽  
...  
Keyword(s):  
Case Report ◽  
Complete Remission ◽  
Adult Patient ◽  
Rare Case ◽  
Embryonal Rhabdomyosarcoma ◽  
Childhood And Adolescence ◽  
Solid Mass ◽  
Mesenchymal Tissue ◽  
Rare Case Report ◽  
Tissue Origin

Rhabdomyosarcoma is a malignancy of mesenchymal tissue origin typically occurring in childhood and adolescence, with an incidence rate of of 4.3 patients per million population per anum. Primary rhabdomyosarcoma of para-testicular origin is an infrequent condition, making up to 7% of all the cases of rhabdomyosarcoma tumors in children and adolescents. Here we describe a case of a 25 years old man with left paratesticular solid mass. He underwent left sided orchiectomy with histopathology revealing paratesticuler embryonal rhabdomyosarcoma. He underwent definitive chemo-radiotherapy and orchidopexy with complete remission and is on active surveillance for 4 years.

scholarly journals Early gallbladder carcinoma with cholelithiasis: a rare case report

2017 ◽  
Vol 4 (7) ◽  
pp. 2363 ◽  
Author(s):  
Senthil Kumar A. C. ◽  
Balamurali S. ◽  
Reshma S.
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Mortality Rate ◽  
Gall Bladder ◽  
Gallbladder Carcinoma ◽  
Bladder Carcinoma ◽  
Rare Case ◽  
Gall Bladder Carcinoma ◽  
Rare Case Report ◽  
Advanced Stages

Gall bladder carcinoma is an exceedingly rare and fatal cancer with a high mortality rate.  Detecting gall bladder carcinoma in early stages can be difficult, despite improvements in ultrasound and computed tomography (CT) imaging. Most diagnoses of gallbladder carcinoma are made at advanced stages, with majority being found incidentally during surgery for cholelithiasis.  The presented case demonstrates suspicion of Gallbladder carcinoma pre-operatively. 

scholarly journals Giant Pelvic Retroperitoneal Epidermoid Cyst: A Rare Case Report

2012 ◽  
Vol 2012 ◽  
pp. 1-4 ◽  
Author(s):  
F. Z. Fdili Alaoui ◽  
A. Oussaden ◽  
H. Bouguern ◽  
H. El Fatemi ◽  
M. A. Melhouf ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Epidermoid Cyst ◽  
Rare Case ◽  
Cutaneous Tumor ◽  
Rare Case Report

Epidermoid cyst is a frequent benign cutaneous tumor. The pelvic localization does not occur very often. The literature that taps into such cases is very limited in scope. Here is a report of a 27-year-old woman with a giant pelvic retroperitoneal epidermoid cyst. The use of ultrasound exploration and computed tomography has indicated ovarian origins. The surgery also revealed a retroperitoneal epidermoid cyst, uterus and ovaries were all intact. The evacuation of a cyst was found to contain lamellas of keratin. Histology permitted us to confirm the diagnosis. The patient was faring well after two years of followup.

scholarly journals Mandibular First Molar with Vertucci Type I Canal Configuration diagnosed with the Help of Cone Beam Computed Tomography: A Rare Case Report

2014 ◽  
Vol 15 (6) ◽  
pp. 784-787
Author(s):  
Manoj Agarwal ◽  
HP Trivedi ◽  
Ankit Gaur ◽  
Manju Gupta ◽  
Anuradha Sharma ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Cone Beam Computed Tomography ◽  
Rare Case ◽  
Three Dimensional ◽  
Anatomical Variations ◽  
Cone Beam ◽  
Type I ◽  
Rare Case Report ◽  
Mandibular First Molar

ABSTRACT The knowledge of root canal morphology and the existing anatomical variations is essential for successful endodontic therapy. This report presents an extraordinary case of unusual tooth morphology involving the mandibular first molar with a single root and a single canal in a patient. Endodontic treatment of the affected tooth 36 was performed. Cone beam computed tomography (CBCT) images confirmed our diagnostic and therapeutic measures after endodontic management of the teeth. This morphologic variation has been reported once in the literature. The availability of three-dimensional images further provided the opportunity for the precise description of the anatomy of mandibular first molar with single roots and single canals. How to cite this article Gaur A, Trivedi HP, Gupta M, Sharma A, Likhyani L, Agarwal M. Mandibular First Molar with Vertucci Type I Canal Configuration diagnosed with the Help of Cone Beam Computed Tomography: A Rare Case Report. J Contemp Dent Pract 2014;15(6):784-787.

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