scholarly journals Rare Case report of Amyand's Hernia in a Premature Infant

2021 ◽  
Vol 8 (5) ◽  
pp. 01-04
Author(s):  
Aiman Rahmani ◽  
Zohra Ashraf Siwji ◽  
Alya Talib AlBlooshi ◽  
Moustafa Hamchou
Keyword(s):  
Premature Infants ◽  
Rare Case ◽  
Common Finding ◽  
Amyand’S Hernia ◽  
Age Group ◽  
Processus Vaginalis ◽  
Rare Finding ◽  
Patent Processus Vaginalis ◽  
Rare Case Report ◽  
Amyand Hernia

Although inguinal hernias are a common finding in premature infants, it is usually caused by the protrusion of the bowel through a persistent patent processus vaginalis. However, acute appendicitis in association with an inguinal hernia in this age group is a rare finding. This type of hernia is referred to as an Amyand hernia.

Right sided Amyand's hernia: a rare case report

2014 ◽  
Vol 1 (1) ◽  
pp. 43 ◽  
Author(s):  
Amit Mahajan ◽  
Pranay Pawar ◽  
Anil Luther ◽  
Parvez Haque
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Amyand’S Hernia ◽  
Rare Case Report

scholarly journals Posttraumatic Chronic Ossified Extradural Hematoma: A Rare Case Report

2014 ◽  
Vol 21 (3) ◽  
pp. 363-365
Author(s):  
Rakesh Kumar ◽  
Radhe Shyam Mittal
Keyword(s):  
Case Report ◽  
Head Injury ◽  
Rare Case ◽  
Temporal Region ◽  
Age Group ◽  
Extradural Hematoma ◽  
Rare Case Report ◽  
Paediatric Age

Abstract Posttraumatic Chronic ossified extradural hematomas are rare entities. Natural absorption of EDH does not occurs due to calcification. Chronic ossified EDH is frequently present in paediatric age group. Careful regular follow-up is mandatory in conservatively managed case of EDH in children. We report a rare case of Posttraumatic Chronic ossified extradural hematomas in a 10-years old girl presenting six years after head injury with right temporal region swelling.

scholarly journals Extensive intramuscular cysticercosis without any neurological involvement: A rare case report

2015 ◽  
Vol 1 (8) ◽  
pp. 313
Author(s):  
Yasmeen Shamsi ◽  
Azhar Jabeen ◽  
Sadia Nikhat ◽  
Shafia Mushtaque
Keyword(s):  
Rare Case ◽  
Incidental Finding ◽  
Subcutaneous Tissue ◽  
Taenia Solium ◽  
The Body ◽  
Neurological Involvement ◽  
Rare Finding ◽  
Systemic Involvement ◽  
Cysticercus Cellulosae ◽  
Rare Case Report

<p>Human cysticercosis is a common tropical disease which is caused by Cysticercus cellulosae, larvae of a tapeworm, Taenia solium. Cysticercosis can involve any tissue in the body; the most common affected sites are central nervous system, subcutaneous tissue, eyes, and muscles. Extensive intramuscular Cysticercosis without any other systemic involvement is a very rare finding. Here, we report a case of intramuscular Cysticercosis incidentally diagnosed by plain radiographs in a 51 year-old man who presented with osteoarthritis right knee joint and Cysticercosis was an incidental finding.</p>

scholarly journals Left sided obstructed Amyand’s hernia: a rare case report

2019 ◽  
Vol 6 (5) ◽  
pp. 1806
Author(s):  
Akash Agrawal ◽  
Palak Vora
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Rare Case ◽  
Perforated Appendicitis ◽  
Amyand’S Hernia ◽  
Right Colon ◽  
Rare Form ◽  
Hernial Sac ◽  
Rare Case Report ◽  
The Right

Amyand's hernia is a rare form of an inguinal hernia (less than 1% of inguinal hernias) which occurs when the appendix is a part of hernial sac. Because of anatomical position of the appendix, it is most commonly found in the right sided hernial sac and it can also be accompanied by the caecum and/or right colon. In rare case, Amyand’s hernia can appear on the left side also. Here we report a case of left sided amyand’s hernia with acute perforated appendicitis in a 58 years old male patient at GMERS hospital, Dharpur, Patan, Gujarat, India.

scholarly journals A Giant Hydatid Cyst at Right Frontoparietal Region: A Rare Case Report

2015 ◽  
Vol 31 (2) ◽  
pp. 116-120
Author(s):  
Haradhan Deb Nath ◽  
Kanak Kanti Barua ◽  
Mohammad Shahnawaz Bari ◽  
Ahmedul Mursalin ◽  
Md Masum Ali
Keyword(s):  
Hydatid Cyst ◽  
Rare Case ◽  
Clinical Findings ◽  
Parasitic Disease ◽  
Limb Weakness ◽  
Rare Finding ◽  
Rare Case Report ◽  
History Of ◽  
The Central Nervous System ◽  
Intracranial Hydatid Cyst

Background: Hydatid cyst is a parasitic disease which can affect the central nervous system. Objective: The purpose of the study is to reveal the clinical findings and the effect of giant the intracranial hydatid cyst at frontoparietal region, which is a rare finding. Results: A patients with right frontoparietal hydatid cyst was admitted in our hospital with history of headache, seizure and left upper limb weakness. We operated the patient and postoperatively developed hydrocephalous and pseudocyst at the site of operation. Cystoperitoneal shunt was done. The patient was medically treated by albendazole. The patient cured postoperatively. Conclusion: Patients with intracranial hydatid cyst can be treated surgically and with albendazole. Bangladesh Journal of Neuroscience 2015; Vol. 31 (2): 116-120

scholarly journals Myxoid Chondrosarcoma of Maxilla in a Pediatric Patient: A Rare Case Report

2016 ◽  
Vol 2016 ◽  
pp. 1-5 ◽  
Author(s):  
Pranali Nimonkar ◽  
Nitin Bhola ◽  
Anendd Jadhav ◽  
Anuj Jain ◽  
Rajiv Borle ◽  
...  
Keyword(s):  
Rare Case ◽  
Postoperative Radiotherapy ◽  
Surgical Excision ◽  
Treatment Modalities ◽  
Age Group ◽  
Myxoid Chondrosarcoma ◽  
Pediatric Age Group ◽  
Maxillary Molars ◽  
Rare Case Report ◽  
Molar Region

Myxoid variant of chondrosarcoma is an uncommon potentially lethal malignant tumor which is even rare in pediatric age group. In the present paper, we report one such case of intermediate grade myxoid chondrosarcoma of left side of maxilla in a 12-year-old girl. The present case had a firm, painless, and lobulated growth in premolar-molar region which was associated with bicortical expansion. Maxillofacial imaging showed ill-defined radiolucency with displaced maxillary molars. Osteolytic changes were evident with the alveolus and walls of maxillary sinus. Owing to the age of the patient, surgical excision was selected as the modality of management followed by postoperative radiotherapy. This report encompasses the entire gamut of clinicopathological, radiological, and treatment modalities employed for chondrosarcoma.

scholarly journals Sinus Histocytosis with Splenomegaly in Children- A Rare Case Report

2019 ◽  
Vol 10 (2) ◽  
pp. 176-178
Author(s):  
Kuntal Roy ◽  
Fabia Hannan Mone ◽  
Syed Khairul Amin ◽  
Md Ekhlasur Rahman ◽  
Soma Halder
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Rare Case ◽  
Treatment Strategies ◽  
The Body ◽  
Age Group ◽  
Medical College ◽  
Rosai Dorfman Disease ◽  
Rare Case Report ◽  
Life Threatening

Sinus Histiocytosis/Rosai-Dorfman Disease (RDD) are benign, rare proliferative disorder caused by over production and accumulation of specific type of white blood cell (Phagocytic Histiocyte) in the lymph nodes of the body. Here, lymphadenopathy mostly painless and commonly found in the neck (cervical) but  may occur in other areas of the body such as skin, lung, central nervous system, kidney (less than 5%). Predominantly it affects the young age group of children, adolescents or young adults. In spite of spontaneous remissions, treatment strategies can be different according to involvement and severity (RDD-  Seldom life threatening disease). Anwer Khan Modern Medical College Journal Vol. 10, No. 2: July 2019, P 176-178

scholarly journals Hydrocele of canal of Nuck in an adult female: a case report

2019 ◽  
Vol 6 (9) ◽  
pp. 3415
Author(s):  
Atish K. Parikh ◽  
Girish D. Bakhshi ◽  
Deepak B. Gadekar ◽  
Kushagra Rahul ◽  
Kritika Garg
Keyword(s):  
Adult Female ◽  
Rare Case ◽  
Inguinal Canal ◽  
Rare Condition ◽  
Age Group ◽  
Pediatric Age ◽  
Serous Fluid ◽  
Processus Vaginalis ◽  
Pediatric Age Group ◽  
Canal Of Nuck

A hydrocele of canal of Nuck is a rare condition seen in females, commonly in the pediatric age group. The canal of Nuck is an extension of peritoneum into the inguinal canal through the deep ring, analogous to the processus vaginalis in males. Incomplete proximal obliteration and collection of serous fluid in the sac leads to the formation of a hydrocele of canal of Nuck. Here we present a rare case of hydrocele of canal of Nuck in an adult female.

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