Volume 9 - Issue 3
Authors : Dr. Mansi Baviskar, Dr. Shilpa Shetty Naik, Dr. Ishani Ratnaparkhi, Dr.Chinmaya Chaudhary*
Primary teeth are the best space maintainers and hence they should be preserved and retained as long as possible. Pulpectomy of primary teeth is indicated when
there is inflammation of the pulpal tissue. The procedure consists of extirpation
of the pulp tissue, filing of the canals to remove organic debris and obturating
with an antibacterial, resorbable paste. Over the years, different materials and
methods have evolved for obturation.
Authors : Naina Joshi, Vijaya Kumar M*
Stroke has been stated as the other leading cause of death and ranked as the third leading source of disability. The WHO explained stroke as
“rapidly developed clinical signs of focal disturbance of cerebral function, lasting further than 24 hours or leading to death, with no apparent cause other than
of vascular origin.” To treat stroke the intravenous thrombolytic program was found to be effective. Orthotics can be used to treat cases with CNS conditions
that are custom-made and prefabricated with variable cost.
Authors : Rajendra Maharjan, Ashish Rouniyar*
Chronic gastritis, an inflammatory condition of the gastric mucosa, can affect different parts of the stomach, causing varying degrees of
mucosal damage. The purpose of this study was to determine the prevalence of histopathological abnormalities among outpatients at a tertiary care center.
Authors : Rajendra Maharjan, Ashish Rouniyar*
Thyroid dysfunction is a prevalent endocrine disorder that can significantly affect metabolic and cardiovascular health. This retrospective
study evaluated the prevalence and patterns of thyroid dysfunction in patients at a clinic in Lalitpur, Nepal, focusing on triiodothyronine (T3), thyroxine (T4),
and thyroid-stimulating hormone (TSH) levels variations.
Authors : Dr Amodini Lakshmeswar*, Dr Madhu Pujar
Neurocutaneous syndromes are a group of disorders with shared embryonic origins involving neural and epidermal tissues. CEDNIK Syndrome
(CErebral Dysgenesis, Neuropathy, Ichthyosis, and Keratoderma) is a rare genetic condition with an estimated global incidence of 0.043%. It results from mutations
in the SNAP29 gene, which is vital for cellular trafficking and other essential processes. These mutations lead to developmental and clinical manifestations,
underscoring the importance of early diagnosis and intervention.
Authors : Yasin Tire, Aydın Mermer
Over the past century, anesthetic has changed dramatically, moving from crude methods to advanced, technologically advanced procedures. The use
of cutting-edge equipment and digital technologies has increased anesthetic care's accuracy, security, and effectiveness. With an emphasis on their effects
on clinical workflows and patient outcomes, this narrative review examines significant technical developments that have influenced contemporary
anesthetic procedures.
Authors : Soukaina Hallouli*, Nabil Bougteb, Wiam El Khattabi, Naima Ait Mouddene, Hajar Arfaoui, Hajar Bamha, Salma Msika, Moulay Hicham Afif
Unilateral pulmonary artery agenesis is a rare malformation affecting 1% of congenital heart diseases. Initially described by Fraentzel in 1868 (1), it is
often asymptomatic but can have a variable clinical presentation. We report two medical cases of two patients aged 69 and 33 years, respectively, presenting
with complicated bronchiectasis that revealed unilateral pulmonary artery hypoplasia. The first patient had left-sided hypoplasia, while the second had
right-sided hypoplasia.
Authors : Danielle Weiss*, Beverley Newman, Terry L. Levin
Congenital peribronchial myofibroblastic tumor (CPMT) is a benign mesenchymal tumor. Due to its rarity and imaging and histologic similarities
with other fetal and neonatal lung lesions, it may be misdiagnosed as a congenital lung malformation or malignant pulmonary neoplasm. CPMT
has been previously reported under a variety of different names including pulmonary hamartoma, bronchopulmonary fibrosarcoma, bronchopulmonary
leiomyosarcoma, congenital fibroleiomyosarcoma and congenital mesenchymal adenomatoid malformation [1, 2].
