scholarly journals Early diagnosis Gorlin-Goltz syndrome: A Rare Case Report

2018 ◽  
Vol 1 (3) ◽  
Author(s):  
Shakhawan M Ali
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Rare Case ◽  
Goltz Syndrome ◽  
Rare Case Report

Gorlin-Goltz syndrome: A rare case report

2016 ◽  
Vol 3 (1) ◽  
pp. 26-30
Author(s):  
Mubeen Khan ◽  
K.R. Vijayalakshmi ◽  
Preeti Rajguru
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Goltz Syndrome ◽  
Rare Case Report

scholarly journals Multiple keratocysts of the mandible in association with Gorlin-Goltz syndrome: A rare case report

2014 ◽  
Vol 5 (3) ◽  
pp. 419 ◽  
Author(s):  
ShahanavajI Khaji ◽  
Suryakant Metkari ◽  
HarishS Kulkarni ◽  
Reshma Kulkarni ◽  
GayithriHarish Kulkarni
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Goltz Syndrome ◽  
Rare Case Report

scholarly journals Early Diagnosis: A Seeming Misfortune for Osteosarcoma of Mandible—Rare Case Report

2018 ◽  
Vol 71 (S1) ◽  
pp. 748-751 ◽  
Author(s):  
Ashvin Wagh ◽  
Gauri Kokane ◽  
Shoeb Jendi ◽  
Shuaib Khatib ◽  
Jagruti Mistry ◽  
...  
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Rare Case ◽  
Rare Case Report

scholarly journals Extrahepatic undifferentiated embryonal sarcoma, cytology as an accurate method for early diagnosis: an extremely rare case report in an Indian child

2019 ◽  
Vol 7 (8) ◽  
pp. 3175
Author(s):  
Nupur Rastogi ◽  
R. K. Tanwar ◽  
B. Saxena
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Rare Case ◽  
Normal Liver ◽  
Accurate Method ◽  
First Case ◽  
Mesenchymal Neoplasm ◽  
Rare Case Report ◽  
Upper Abdominal ◽  
Embryonal Sarcoma

Undifferentiated embryonal sarcoma has been described in the liver, a rare malignant mesenchymal neoplasm, that occurs primarily in children and teenagers. Approximately 260 cases have been reported arising in the liver since 1978 when this disease was first described. Its pathogenesis is still obscure. Authors presented a case of extrahepatic undifferentiated embryonal sarcoma in a 9-year-old female presenting with upper abdominal dull pain. Ultrasound and CT Scan showed normal liver architecture, with liver pushed upwards due to compression by tumor arising in the retroperitoneum. To the best of our knowledge, this is first case of extrahepatic undifferentiated embryonal sarcoma diagnosed on cytomorphology and confirmed by histopathology and immunohistochemistry markers.

scholarly journals A Rare Case Report on Thoracoomphalopagus

2016 ◽  
Vol 11 (1) ◽  
pp. 62-64
Author(s):  
Sabina Lamichhane ◽  
B Banerjee ◽  
S Subedi
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Rare Case ◽  
Pregnancy Termination ◽  
Conjoined Twins ◽  
Second Trimester ◽  
Mortality And Morbidity ◽  
Rare Case Report ◽  
Present Case Study

In the present case study we are reporting a case of thoracoomphalopagus conjoined twins. A 24 years old gravida two para 0+1 carrying thoracoomphalopagus conjoined twins was diagnosed by ultrasonography at early second trimester with single placenta attached posteriorly and low lying. The mortality and morbidity of conjoined twins are high so making the early diagnosis with ultrasonographic examination provides the parents a chance to elect for pregnancy termination.

scholarly journals Gorlin-Goltz syndrome: A rare case report

2013 ◽  
Vol 4 (4) ◽  
pp. 547 ◽  
Author(s):  
ChetanA Pol ◽  
SuvarnaK Ghige ◽  
RiteshR Kalaskar ◽  
SuchitraR Gosavi
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Goltz Syndrome ◽  
Rare Case Report

scholarly journals Renal Endometriosis Tends to Be Misdiagnosed as Renal Tumor: A Rare Case Report

2015 ◽  
Vol 100 (2) ◽  
pp. 376-380 ◽  
Author(s):  
Jie Yang ◽  
Ri-jin Song ◽  
Chen Xu ◽  
Shi-qing Zhang ◽  
Wei Zhang
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Case History ◽  
Rare Case ◽  
Renal Tumor ◽  
Final Diagnosis ◽  
Histopathologic Examination ◽  
Menstrual Cycles ◽  
Appropriate Treatment ◽  
Rare Case Report

Renal endometriosis is a rare disease for which the mechanisms of pathogenesis are still unclear. As such, early diagnosis and an appropriate treatment are often delayed because of the tendency to be misdiagnosed as a renal tumor. In October 2013 we performed a radical nephrectomy for a 37-year-old woman with renal endometriosis who was preoperatively misdiagnosed as having a right renal tumor. Avoiding the misdiagnosis of renal endometriosis requires a detailed case history, especially regarding whether the cyclicity of lumbodorsal pain and hematuria correlates with patients' menstrual cycles. Imaging examinations are commonly helpful for localization, whereas relieving symptoms with drugs to create a hypoestrogenic state is useful for clinical diagnosis. However, a final diagnosis for renal endometriosis still must depend on histopathologic examination.

Early diagnosis of body stalk anomaly – a rare case report

2018 ◽  
Vol 67 ◽  
pp. S14
Author(s):  
S.R. Seema ◽  
A.M. Raja ◽  
Sujit Kumar
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Rare Case ◽  
Rare Case Report
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