scholarly journals Tuberculous Osteomyelitis of Mandible: A Rare Case Report

2018 ◽  
Vol 5 (1) ◽  
pp. 59-62
Author(s):  
Ravish Mishra ◽  
B B Mall ◽  
Laxmi Kandel ◽  
Santoh Kandel
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Condition ◽  
Medical Sciences ◽  
Neoplastic Diseases ◽  
Rare Case Report ◽  
Tuberculous Osteomyelitis ◽  
Primary Focus

Tuberculous osteomyelitis of mandible is an extremely rare condition, particularly in comparison to pyogenic infections and neoplastic diseases involving the mandible. Hereby we are reporting such type of case in a ten year old male, presented with draining sinus over right mandible since 3 months proved later as tuberculous osteomyelitis in absence of a primary focus and responded well to antitubercular treatment.Journal of Universal College of Medical Sciences (2017) Vol.05 No.01 Issue 15, Page: 59-62 

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 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 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 Anterior Chest wall Cold Abscess at Alluri Sita Rama Raju Academy of Medical Sciences, Eluru

2014 ◽  
Vol 2 (1) ◽  
pp. 61
Author(s):  
J R K Lande ◽  
K Chandra Sekhar ◽  
Narendra Valluri ◽  
Siva Rama Prasad Komera ◽  
P G Deotale
Keyword(s):  
Case Report ◽  
Chest Wall ◽  
Rare Case ◽  
Anterior Chest Wall ◽  
Medical Sciences ◽  
Cold Abscess ◽  
Rare Case Report

scholarly journals Tuberculous osteomyelitis affecting periodontium: A rare case report

2015 ◽  
Vol 19 (5) ◽  
pp. 578 ◽  
Author(s):  
Gaurav Bakutra ◽  
Balaji Manohar ◽  
Lalit Mathur
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Case Report ◽  
Tuberculous Osteomyelitis

scholarly journals Hypercalcemia in a patient with SLE and antiphospholipid antibody syndrome: a rare case report from Bangladesh

2014 ◽  
Vol 2 (1) ◽  
pp. 35-37
Author(s):  
G Dewan
Keyword(s):  
Case Report ◽  
Primary Hyperparathyroidism ◽  
Rare Case ◽  
Adult Patients ◽  
Antiphospholipid Antibody ◽  
Antiphospholipid Antibody Syndrome ◽  
Medical Sciences ◽  
Rare Presentation ◽  
Initial Report ◽  
Rare Case Report

Association of hypercalcemia with SLE is very rare. Since initial report in 1991 only hand full cases have been described mainly in adult patients sporadically. Three pattern observed in this rare presentation. Commonly it is associated with serositis and lymphadenopathy or lymphedema known as hypercalcemia-lymphadenopathy SLE {HL-SLE) or hypercalcemia- lymphedema syndrome. Second group do not show this particular association. Concomitant primary hyperparathyroidism is responsible for third variety. This report describes a case of hypercalcemia associated with SLE from Bangladesh. DOI: http://dx.doi.org/10.3126/jucms.v2i1.10490   Journal of Universal College of Medical Sciences (2014) Vol.2(1): 35-37

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 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.

scholarly journals Submandibular Abscess due to an Infected Keratocystic Odontogenic Tumor associated with Simultaneous Occurrence of a Traumatic Bone Cyst: A Rare Case Report

2013 ◽  
Vol 14 (1) ◽  
pp. 133-136 ◽  
Author(s):  
Poorandokht Davoodi ◽  
Loghman Rezaei-Soufi ◽  
Mina Jazaeri ◽  
Adineh Javadian Langaroodi ◽  
Seyed Hossein Hoseini Zarch
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Present Report ◽  
Bone Cyst ◽  
Rare Condition ◽  
Odontogenic Tumor ◽  
Simultaneous Occurrence ◽  
Keratocystic Odontogenic Tumor ◽  
Submandibular Region ◽  
Rare Case Report

ABSTRACT Aim The aim of this report is to introduce a rare case in which an infected keratocystic odontogenic tumor (KCOT) was initially diagnosed and treated as a dentoalveolar abscess. Background Keratocystic odontogenic tumor (KCOT) is a benign neoplasm that can be secondarily infected. However, cervical soft tissue abscess formation as a result of an infected odontogenic cyst or tumor is a rare condition few of which have only been described in the existing literature. Also, there has been a single report regarding the coincidence of a traumatic bone cyst and a keratocytic odontogenic tumor to date. Case report The patient was a 29-year-old male, complaining of fever, pain and swelling in the left submandibular region. The panoramic radiography showed a well-defined and partially corticated radiolucency between the roots of the second and third left mandibular molars. In addition, a well-corticated radiolucent lesion was incidentally found on the right side of the mandible, which, following surgical exploration, was diagnosed as a traumatic bone cyst. Conclusion In the present report, an infected KCOT manifested as a cervical abscess, coincided with a traumatic bone cyst. Clinical significance From the clinical point of view, it is of paramount significance to prevent misdiagnosis of similar presentations as pulp and periapical lesions, which may lead to mistreatment and thus complications. How to cite this article Davoodi P, Rezaei-Soufi L, Jazaeri M, Javadian Langaroodi A, Hoseini Zarch SH. Submandibular Abscess due to an Infected Keratocystic Odontogenic Tumor associated with Simultaneous Occurrence of a Traumatic Bone Cyst: A Rare Case Report. J Contemp Dent Pract 2013;14(1): 133-136.

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