scholarly journals A RARE CASE OF EMPHYSEMATOUS PANCREATITIS: A CASE REPORT

2020 ◽  
Vol 4 (12) ◽  
Author(s):  
Hemant L Leuva ◽  
Jainam K Shah ◽  
Jigar Vitthalbhai Paghadar ◽  
Parli Kanak Kothari ◽  
Shubham Garg ◽  
...  
Keyword(s):  
Case Report ◽  
Male Patient ◽  
High Mortality ◽  
Rare Case ◽  
Epigastric Pain ◽  
Rare Complication ◽  
Necrotizing Infection ◽  
Surgical Emergency

High mortality is noted with a rare complication of pancreatitis also known as emphysematous pancreatitis. Here we present a rare case of a 40 years old male patient presented with complain of epigastric pain. It is considered as a surgical emergency. Keywords: mortality, surgery, emphysematous pancreatitis, necrotizing infection

scholarly journals Pseudomyxoma pleuri as a Surgical Emergency: a Rare Case Report

2017 ◽  
Vol 9 (2) ◽  
pp. 271-273
Author(s):  
Deepak K. Sharma ◽  
Dharma Ram ◽  
Himanshu Shukla ◽  
Suhas Kodasoge Rajappa ◽  
L. M. Darlong
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Surgical Emergency ◽  
Rare Case Report

scholarly journals Pyogenic granuloma of tongue: A rare case report

2014 ◽  
Vol 6 (3) ◽  
pp. 84-86
Author(s):  
Sonam Sharma ◽  
Amita Sharma ◽  
Ashok Kumar ◽  
Shivani Kalhan ◽  
Jasmine Kaur
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Male Patient ◽  
Rare Case ◽  
Pyogenic Granuloma ◽  
Definitive Diagnosis ◽  
Medical Sciences ◽  
New Approaches ◽  
Rare Case Report ◽  
Chronic Irritation

Pyogenic granuloma (PG) is a kind of inflammatory hyperplasia in response to chronic irritation. Here, we report a case of 64 year old male patient with PG on midline of the dorsum of the posterior third of the tongue. Its differential diagnosis, the importance of biopsy findings in establishing definitive diagnosis and about the new approaches for its treatment is discussed. DOI: http://dx.doi.org/10.3126/ajms.v6i3.10619Asian Journal of Medical Sciences Vol.6(3) 2015 84-86

scholarly journals Ventricular Septal Rupture Secondary to Myocardial Infarction Post Fibrinolytic Therapy: A Case Report

2019 ◽  
Author(s):  
Ankitha Peetha ◽  
Nahida Farheen Shaik ◽  
Spandana Ayela
Keyword(s):  
Myocardial Infarction ◽  
Case Report ◽  
Mortality Rate ◽  
High Mortality ◽  
Anterior Wall ◽  
Fibrinolytic Therapy ◽  
Mechanical Complication ◽  
Ventricular Septal Rupture ◽  
Surgical Emergency

Myocardial infarction can be complicated by Ventricular septal rupture which is a rare fatal grim mechanical complication of MI which is a surgical emergency due to its incredibly high mortality rate. We depict a case of Anterior wall MI which was complicated by Ventricular septal rupture post fibrinolytic therapy.

scholarly journals Reversed rotation of the midgut in adults – a case report

2010 ◽  
Vol 92 (7) ◽  
pp. e3-e5 ◽  
Author(s):  
Hany Balamoun ◽  
Robina Mohammad ◽  
Ayman Hamade
Keyword(s):  
Case Report ◽  
Intestinal Obstruction ◽  
Rare Case ◽  
Surgical Emergency ◽  
Reversed Rotation

Intestinal obstruction is a common surgical emergency. It is often due to adhesions; however, when the patient is young and has a virgin abdomen, we have to consider uncommon causes. We present a rare case of reversed rotation of the midgut as a cause for intestinal obstruction.

scholarly journals AGGRESSIVE MESENTRIC FIBROMATOSIS: A RARE CASE REPORT AND REVIEW OF LITERATURE

2013 ◽  
Vol 03 (01) ◽  
pp. 79-82
Author(s):  
Rohan Shetty ◽  
Shubha Bhat ◽  
Rajesh Ballal ◽  
Pramod Makannavar ◽  
Anil Kumar K. N.
Keyword(s):  
Case Report ◽  
Male Patient ◽  
Rare Case ◽  
Clinical Presentation ◽  
Aggressive Fibromatosis ◽  
Definitive Diagnosis ◽  
Review Of Literature ◽  
Therapeutic Challenge ◽  
Rare Case Report ◽  
Small Intestinal

AbstractMesentric fibromatosis is a proliferative fibroblastic neoplasm of the small intestinal mesentery with varied clinical presentation. Giant mesentric fibromatosis is uncommon and its rarity poses a diagnostic and therapeutic challenge. This paper presents a recurrent aggressive fibromatosis in a 38 year old male patient, who had initially undergone a laparotomy outside for mass abdomen but only pus was evacuated and definitive diagnosis was not made.

Retroperitoneal hematoma — a rare complication after cervical conization because of cervicoisthmic arteriovenous malformation: a case report

Open Medicine ◽  
2011 ◽  
Vol 6 (6) ◽  
pp. 710-712
Author(s):  
Dubravko Habek ◽  
Tatjana Turudić
Keyword(s):  
Risk Factor ◽  
Case Report ◽  
Arteriovenous Malformation ◽  
Rare Case ◽  
Rare Complication ◽  
Retroperitoneal Hematoma ◽  
Retroperitoneal Hemorrhage ◽  
Cold Knife ◽  
Cold Knife Conization ◽  
Cervical Conization

AbstractA rare case is presented concerning retroperitoneal hemorrhage in a 28-year-old patient after a cold knife conization and cervical suture reconstruction. Arteriovenous cervicoisthmic malformation is a risk factor that was identified in a hysterectomy sample.

Large and Long Standing Cavernous Hemangioma of Cheek

2013 ◽  
Vol 5 (2) ◽  
pp. 91-93
Author(s):  
Hitesh Verma
Keyword(s):  
Case Report ◽  
Male Patient ◽  
Cavernous Hemangioma ◽  
Rare Case ◽  
Vascular Malformations ◽  
Large Size ◽  
Cavernous Hemangiomas

ABSTRACT Cavernous hemangiomas are relatively rare vascular malformations especially in an adult. The childhood hemangioma generally regresses spontaneously. We present the case report of a 52-year-old male patient, who had a hemangioma from the childhood and it had grown to such a large size so as to cause extreme cosmetic deformity for the patient. The long standing duration of almost 45 years and the extremely large size of the hemangioma make it a very rare case. How to cite this article Gupta N, Verma H. Large and Long Standing Cavernous Hemangioma of Cheek. Int J Otorhinolaryngol Clin 2013;5(2):91-93.

scholarly journals Congenital Microphthalmia with Intraorbital Cyst: A Rare Case Report

2019 ◽  
Vol 2019 ◽  
pp. 1-3
Author(s):  
Bishow Raj Timalsina ◽  
Gulshan Bahadur Shrestha ◽  
Madhu Thapa
Keyword(s):  
Case Report ◽  
Congenital Malformation ◽  
Male Patient ◽  
Rare Case ◽  
Congenital Cataract ◽  
Orbital Tumor ◽  
Rare Case Report

Microphthalmia is considered to be the most common congenital malformation of the eye after congenital cataract. However, its association with intraorbital cyst is considered to be very rare. Most of the lesions are still misdiagnosed as orbital tumor and teratomas as there is a general paucity of data reported in literature. Herein, we report a rare case of congenital microphthalmia with intraorbital cyst in an eight-month-old male patient.

scholarly journals Lipoma in Penis : A Rare Case Report

2013 ◽  
Vol 3 (1) ◽  
pp. 24-25
Author(s):  
T Ahmed ◽  
MA Kalam ◽  
II Mannan ◽  
MA Simi
Keyword(s):  
Case Report ◽  
Plastic Surgery ◽  
Male Patient ◽  
Rare Case ◽  
Young Male ◽  
Histopathological Analysis ◽  
Review Of The Literature ◽  
Ventral Aspect ◽  
Rare Case Report ◽  
Pedunculated Tumor

In this article we report one case of lipoma of the penis in a twenty three years old young male. This site of lipoma is rare. A case of a young male patient who consulted for removal of a penile lump is presented. The small, regular, wellcircumscribed pedunculated tumor localized on the ventral aspect of the penis was excised. The histopathological analysis showed a benign lipoma. A review of the literature showed lipoma of the penis to be very uncommon. For this reason, we were prompted to report this case.DOI: http://dx.doi.org/10.3329/bdjps.v3i1.15003 Bangladesh Journal of Plastic Surgery 2012, 3(1): 24-25

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