scholarly journals Multiple epidermal cysts of the scrotum: a rare case report

2017 ◽  
Vol 4 (7) ◽  
pp. 2375 ◽  
Author(s):  
Yeshwant Kumar N. N. T. ◽  
Reshma S. ◽  
Deivanayagam S.
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Surgical Intervention ◽  
Rare Condition ◽  
Complete Excision ◽  
Rare Case Report

Multiple epidermal cysts over the scrotum is a rare condition and requires surgical intervention if infected or cosmetically unacceptable.  Grossly enlarged cysts require complete excision, followed by scrotoplasty.  We are reporting a case of multiple epidermal cysts on the scrotum.  Complete excision of the cysts followed by scrotoplasty was done in this case.

scholarly journals Omental lymphangioma: a rare case report

2020 ◽  
Vol 10 (3) ◽  
pp. 106-108
Author(s):  
Geha Raj Dahal
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Rare Case ◽  
Neck Region ◽  
Mass Effect ◽  
Complete Excision ◽  
Benign Condition ◽  
Head And Neck Region ◽  
Rare Case Report

Lymphangioma is a common pediatric problem. Most of the lymphangiomas occur in head and neck region. Lymphangioma arising from omentum is extremely rare. It is a benign condition butis locally invasive. Symptoms usually arise from its mass effect or complications. Complete excision including removal of all loculi is necessary for cure. We report such a case of omental lymphangiomain a six-year boy.

scholarly journals Fetus papyraceus: a rare case report

2020 ◽  
Vol 7 (1) ◽  
pp. 113-116
Author(s):  
Namita Sindan ◽  
Adheesh Bhandari ◽  
Snigdha Rai ◽  
Devi Gurung
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Fetal Death ◽  
Rare Condition ◽  
Positive Outcome ◽  
Uterine Wall ◽  
Anatomical Location ◽  
Multiple Gestations ◽  
Gynecology And Obstetrics ◽  
Rare Case Report

Fetus papyraceus is a rare condition of a mummified and compressed fetus occurring in multiple gestations where one fetus dies in utero and is merged between the uterine wall and the membranes of living fetus. The blood vessels of the placenta of the two fetuses anastomose with each other, a third cycle occurs, causing fetal death (fetal transfer syndrome). Ultrasonography may identify the Fetus papyraceus, but is not always promising due to anatomical location. Cautious supervision is important during pregnancy for its positive outcome. We report a case of fetus papyraceus in Department of Gynecology and Obstetrics, Paropakar Maternity and Women’s Hospital, Kathmandu, Nepal.

A rare case report of neonatal iliopsoas abscess presenting as swelling of left hip

2020 ◽  
pp. 1-6
Author(s):  
Maimoona Saeed ◽  
Iqtada Haider Shirazi
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Clinical Presentation ◽  
Psoas Abscess ◽  
Rare Condition ◽  
Medical Sciences ◽  
Rare Case Report ◽  
Key Words Abscess ◽  
Systemic Antibiotics ◽  
Bluish Discoloration

Abstract We report the case of a 12 days old baby boy who presented with swelling and bluish discoloration on his left hip at Pakistan Institute of Medical Sciences in November 2018. Ultrasound (USS) was useful in making the diagnosis of a neonatal psoas abscess. He was treated with extraperitoneal drainage and with systemic antibiotics. The clinical presentation and diagnosis, treatment of this rare condition and brief literature review is given in this case report. Key Words: Abscess, Iliopsoas, Neonate, Staphylococcus aureus, Extraperitoneal Drainage. Continuous....

scholarly journals Spinal dysraphism with tripedus morphology: A case report

2021 ◽  
pp. 509-511
Author(s):  
Mohd Monis ◽  
Shagufta Wahab ◽  
Divyashree Koppal ◽  
Aiman Ibbrahim
Keyword(s):  
Case Report ◽  
Spina Bifida ◽  
Vertebral Column ◽  
Rare Case ◽  
Surgical Intervention ◽  
Spinal Dysraphism ◽  
Tethered Cord ◽  
Lower Back ◽  
Rare Case Report ◽  
Spinal Mri

This is a rare case report of a 5-month-old child with a complex spinal dysraphic state, and an accessory limb (tripedus morphology), accessory genitalia, and anal dimple. The child was brought to the hospital with an accessory limb arising from the back. On clinical examination, an accessory limb arising from the lower back with a partially developed foot with the presence of toes and nails was noted. Spinal MRI was advised which revealed dysraphic features including spina bifida with the low lying and posteriorly tethered cord with diastematomyelia along with a supernumerary appendage attached to the vertebral column having rudimentary bones resembling those of extremities. The presence of an accessory limb with spinal dysraphism is quite a rare anomaly. The condition can be treated by surgical intervention and involves excision of the accessory limb with adequate dural and paraspinal muscle cover.

scholarly journals A rare case report of aplasia cutis congenita of the scalp with triplet skin defects in non-syndromic newborn

2021 ◽  
Vol 8 (3) ◽  
pp. 997
Author(s):  
Naim Sulaiman Abuzarifa ◽  
Wan Azman Wan Sulaiman
Keyword(s):  
Case Report ◽  
Gestational Age ◽  
Rare Case ◽  
Surgical Intervention ◽  
Skin Condition ◽  
Skin Defect ◽  
Aplasia Cutis Congenita ◽  
Skin Defects ◽  
Rare Case Report ◽  
Aplasia Cutis

Aplasia cutis congenita is an uncommon localized or widespread congenital skin condition characterized by the absence of the skin, and occasionally underlying tissues occurs in about one every 10.000 birth mostly in the scalp as single or more than one lesion and sometimes occurs in extremities and trunk with an uncertain cause and can be associated with numerous syndromes or can be sporadic which is diagnosed clinically and usually conservatively managed but sometimes surgical intervention needed. In this literature, we present nonsyndromic newborn Malay girl normally delivered with 35 weeks gestational age with triplet skin raw areas at the vertex of the scalp with well-demarcated defect round in shape measured about 0.5 in radius covered with a noninflammatory, necrotic patch. To our knowledge, many works of literatures presented Aplasia cutis congenita at the scalp with solitary single or occasionally more than one skin defect. In contrast, in our case, we present an infrequent rare case of triplet skin defect of aplasia cutis congenita for nonsyndromic newborns. 

scholarly journals Idiopathic Haemolacria: A Rare Case Report

2019 ◽  
Vol 20 (2) ◽  
pp. 106-108
Author(s):  
Goutam Kumar Acherjya ◽  
Mohammad Ali ◽  
Keya Tarafder ◽  
Mostofa Kamal Chowdhury ◽  
Md Abdus Salam ◽  
...  
Keyword(s):  
Case Report ◽  
Malignant Melanoma ◽  
Medical Practice ◽  
Rare Case ◽  
Epstein Barr Virus ◽  
Rare Condition ◽  
Thrombocytopenic Purpura ◽  
Barr Virus ◽  
Rare Case Report ◽  
Epstein Barr

Crying with bloody tear, called haemolacria is a very rare condition in medical practice. There are many conditions such as idiopathic thrombocytopenic purpura, trauma (accidental or induced), factors deficiencies, infections (Epstein Barr virus or bacterial), tumours (malignant melanoma or haemangioma), conjunctival telangiectasia, Rendu-Oslar-Weber disease related to haemolacria. But idiopathic haemolacria may occur in some cases. In our case report, a 17-year-old girl presented with idiopathic bilateral haemolacria and gum bleeding associated with pseudoseizure and psychogenic hyperventilation who was treated and well responded to adequate counselling and Amitriptyline. J MEDICINE JUL 2019; 20 (2) : 106-108

scholarly journals An Asymptomatic Pointed Foreign Body in the Hypopharynx-A Rare Case Report

2016 ◽  
Vol 24 (2) ◽  
pp. 100-105
Author(s):  
Jyotiranjan Das ◽  
Debangshu Ghosh ◽  
Jayanta Saha ◽  
Sumit Kumar Basu
Keyword(s):  
Case Report ◽  
Foreign Body ◽  
Postoperative Period ◽  
Rare Case ◽  
Surgical Intervention ◽  
Magill Forceps ◽  
The Past ◽  
Rare Case Report ◽  
Significant Symptom ◽  
Surgical Option

Introduction Foreign body ingestion is an ENT emergency frequently encountered in both children and adults. Case Report A case of an open safety pin in the hypopharynx in a fifteen year old boy is reported, which remained impacted there for the past 15 days without any significant symptom or complication. CT scan, performed before surgical intervention, did not show any migration of this foreign body from its intraluminal site. This was removed by ‘Magill forceps technique’. Postoperative period was uneventful. Conclusion Pointed foreign body may present with negligible symptoms and that too may stay in the cricopharynx for long without migration. Magill forceps technique can be a good surgical option in such cases.

scholarly journals A rare case of symphalangism of bilateral interphalangial joint of thumbs: a case report

2020 ◽  
Vol 7 (4) ◽  
pp. 1307
Author(s):  
Anil Kumar
Keyword(s):  
Case Report ◽  
Functional Impairment ◽  
Rare Case ◽  
Surgical Intervention ◽  
Rare Condition ◽  
Congenital Disorder ◽  
Rare Congenital Disorder ◽  
Hands And Feet

Symphalangism is rare congenital disorder characterised by ankylosis of interphalangeal joints of hands and feet. The fusion can involve the proximal or the distal joints; however, involvement of the proximal interphalangeal joints is more common. There may other associated skeletol and non-skeletol abnormalities. Here the author reports a 14 year old girl with symphalangism involving the interphalangeal joints of the thumbs of bilateral hand. She did not have any functional impairment and hence no medical or surgical intervention was performed. As involvement of thumbs is very rare condition, author would like to report it. 

scholarly journals Actinomycotic lacrimal canaliculitis: a rare case report

2019 ◽  
Vol 6 (3) ◽  
pp. 973
Author(s):  
Humaira Bashir ◽  
Asifa Nazir
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Opportunistic Infections ◽  
Rare Condition ◽  
Commensal Bacteria ◽  
Epithelial Lining ◽  
Gram Positive ◽  
Anaerobic Organism ◽  
Rare Case Report

Actinomyces israelii is a gram-positive anaerobic organism commonly associated with canaliculitis in adults. Actinomyces are normal commensal bacteria in humans and primarily cause opportunistic infections during immunosuppressive state or when loss of continuity of epithelial lining in mucosa occurs. Lacrimal canaliculitis is a relatively rare condition and is undiagnosed for long periods of time. Being a relatively rare condition, it is commonly overlooked and undiagnosed for long periods of time. Primary chronic canaliculitis is an uncommon problem and Actinomycosis may form in up to 2% of all lacrimal disease. Here present study reports a case of lacrimal canaliculitis caused by Actinomyces israelii.

scholarly journals Odontogenic Fibromyxoma of Maxilla: A Rare Case Report

2015 ◽  
Vol 8 (2) ◽  
pp. 84-88
Author(s):  
Chandra Kant ◽  
Virendra Kumar Prajapati ◽  
Vishwambhar Singh ◽  
Krishna Murari Tiwari
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Posterior Part ◽  
Rare Condition ◽  
Conventional Radiography ◽  
En Bloc Resection ◽  
Bloc Resection ◽  
En Bloc ◽  
Rare Case Report ◽  
Rare Benign Tumor

ABSTRACT Odontogenic fibromyxoma, a myxoma with abundant collagen fibers, is a rare benign tumor of jaw which mostly affects posterior part of mandible. It is ectomesenchymal in origin and probably arises from connective tissue of dental follicle or papilla. Commonly occurs in 2nd or 3rd decade with slight female predilection. Radiological investigations, such as conventional radiography, computed tomography (CT) scan or magnetic resonance imaging (MRI) can be used to differentiate it from other odontogenic tumors like ameloblastoma. Management is surgical by enucleation and curettage or by en bloc resection and segmental maxillectomy. Follow-up of patient is must for at least 2 years to diagnose any recurrence. In this article, we present fibromyxoma of maxilla which is a very rare site for occurrence of fibromyxoma and this relatively rare condition has been discussed in light of recent information from literature with a case report. How to cite this article Kant C, Prajapati VK, Singh V, Tiwari KM. Odontogenic Fibromyxoma of Maxilla: A Rare Case Report. Clin Rhinol An Int J 2015;8(2):84-88.

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