C. Sutterlin, Jane E. Luscombe, Jerry Day, A. Dubey
{"title":"Lateral lumbar interbody fusion (LLIF): Technique and outcomes","authors":"C. Sutterlin, Jane E. Luscombe, Jerry Day, A. Dubey","doi":"10.3126/GMJ.V1I1.22399","DOIUrl":"https://doi.org/10.3126/GMJ.V1I1.22399","url":null,"abstract":"Introduction: Historically, an interbody device (IBD) has consisted of morselized autograft1, structural autograft, structural allograft, stainless steel ball, threaded titanium cage, polyetheretherketone (PEEK) cage, and more recently 3D printed titanium cage with bioactive surface characteristics and bony ingrowth into IBD interstices. These IBD’s have been inserted through a variety of approaches, both by open technique and by minimally invasive surgical (MIS) technique. Traditionally, the most common procedures have been posterior lumbar interbody fusion (PLIF), transfacetal lumbar interbody fusion (TLIF), and anterior lumbar interbody fusion (ALIF). Obviously, both PLIF and TLIF are posterior approaches, and ALIF is an anterior approach. More recent approaches in the retroperitoneal space anteriorly are oblique lumbar interbody fusion (OLIF) anterior to the psoas muscle, and lateral lumbar interbody fusion (LLIF) which is a transpsoas procedure. LLIF is the subject of this manuscript. The LLIF technique utilizing K2M’s Ravine retractor system and K2M’s lateral IBD’s, Aleutian (PEEK) and Cascadia (3D printed titanium) will be described (K2M, Leesburg, VA USA). Bone graft substitute, iFactor (Cerapedics, Colorado USA), was used in all cases. No autograft was harvested from the iliac crest, but local morselized autograft was utilized if available. The clinical outcomes for LLIF using these implants and instruments will be reported.","PeriodicalId":314361,"journal":{"name":"Grande Medical Journal","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"117025784","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Acquired B antigen in ABO blood group system: Non-secretor group 'A1' subtype, Rh positive with auto antibodies in a patient with urinary tract infection with E. coli","authors":"B. Nepal, B. Shrestha, Ravi Mahat, Abish Adhikari","doi":"10.3126/GMJ.V1I1.22411","DOIUrl":"https://doi.org/10.3126/GMJ.V1I1.22411","url":null,"abstract":"This is case report of a female with “A” sub type with acquired B antigen and non-secretor status, first ever reported with this combination in Nepal, during blood grouping of a sample of a patient with urinary tract infection. The patient was referred to our center for blood grouping, cross matching and transfusion due to severe anemia. \u0000During routine blood grouping, the red cells showed mixed field agglutination with anti-A, anti- AB and microscopic agglutination with anti-B. On serum grouping, we detected potent Anti-B and no agglutination with anti-A. There was no reaction with anti-A both at room temperature and at 37°C. Her cells were further tested with A1 Lectin and Anti-H antisera. There was strong reaction with A1 Lectin and 3+ macroscopic reaction with anti-H in addition to a positive auto-control. Her direct antiglobulin test was only +1 positive. For her “B” antigen, we acidified B antisera with HCl, which did not give any macro or microscopic agglutination with patient’s red cells. Her “Rh” status was positive and on examining the saliva, she was found to be non-secretor. \u0000The first choice of blood group for transfusion in this case is the “A1” sub type followed by “O” blood group. As the patient had already received “A” blood group and in the presence of auto antibodies, “A subgroup” blood transfusion should be avoided in her.","PeriodicalId":314361,"journal":{"name":"Grande Medical Journal","volume":"18 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123630318","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Rudimentary third arm arising from the upper back: A rare case","authors":"R. Adhikari, Amit Thapa, C. Pandey","doi":"10.3126/GMJ.V1I1.22405","DOIUrl":"https://doi.org/10.3126/GMJ.V1I1.22405","url":null,"abstract":"We report a case of a 2-year-old boy with rudimentary third arm arising from the dorsal spine with associated spinal dysraphism.","PeriodicalId":314361,"journal":{"name":"Grande Medical Journal","volume":"54 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133885224","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Myometrial myxoidosis: A rare case seen in a patient of primary subfertility","authors":"Nilam Subedi, P. Pant, A. Ghimire","doi":"10.3126/GMJ.V1I1.22420","DOIUrl":"https://doi.org/10.3126/GMJ.V1I1.22420","url":null,"abstract":"Myxoid mesenchymal lesions of the uterus are generally restricted to tumors. Myometrial myxoidosis is a rare benign tumor of the uterus. We report a case of myometrial myxoidosis diagnosed postoperatively with histopathological report in a 27-year-old female with primary subfertility who had undergone myomectomy and adenomyomectomy. On gross examination the tumor was 13.5x8x2.5 cm in size. Microscopically, it showed interlacing bundles of smooth muscles intersecting each other. Sections from separate tissue showed muscle fascicles which were separated by abundant extracellular mucin producing a striking myxoid appearance (myxoidosis). \u0000Only few cases of myometrial myxoidosis have been reported in literature. Of them, some were associated with lupus erythematosus and some with neurofibromatosis.","PeriodicalId":314361,"journal":{"name":"Grande Medical Journal","volume":"108 1-2 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124341623","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Dacryocele in an adult presenting as facial cellulitis","authors":"P. Kansakar, G. Sundar","doi":"10.3126/GMJ.V1I1.22412","DOIUrl":"https://doi.org/10.3126/GMJ.V1I1.22412","url":null,"abstract":"A 47-year-old male presented with left sided facial cellulitis of one-week duration associated with a painful mass over the left medial canthal area. On examination, there was a firm, tender mass below the medial canthal tendon. Computed tomography scan revealed a bulky, cystic lesion at the left inferomedial orbit and medial maxilla with bony remodeling suggestive of a chronic dacryocele. The patient underwent marsupialization of the dacryocele at the inferior meatus with silicone tube intubation. His symptoms of epiphora resolved after surgery. \u0000We describe a rare clinical presentation of dacryocele in an adult and its simple, yet effective treatment option.","PeriodicalId":314361,"journal":{"name":"Grande Medical Journal","volume":"28 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126774696","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Breast cancer during pregnancy","authors":"S. Acharya, Aarati Shah","doi":"10.3126/GMJ.V1I1.22414","DOIUrl":"https://doi.org/10.3126/GMJ.V1I1.22414","url":null,"abstract":"Breast cancer during pregnancy is rare accounting for 1 in around 3000 pregnant women as per the American cancer society. According to hospital-based cancer registry of Nepal, breast cancer accounts for 9.2% of total cancer cases and pregnancy associated breast cancer accounts for 0.15% of the total breast cancer. Though rare, breast cancer is the most common type of cancer found during pregnancy and that too in advanced stage because of the hormonal interplay during pregnancy. Here we present a case of breast cancer during pregnancy which was treated successfully with chemotherapy, surgery, radiation therapy and is on hormonal treatment. Patient is on regular follow up for the last six years without evidence of recurrence of the disease, and the baby has achieved normal developmental milestones though exposed to chemotherapy in utero.","PeriodicalId":314361,"journal":{"name":"Grande Medical Journal","volume":"7 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127595271","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Trends of laparoscopic gynecologic surgeries in a tertiary care center: A five-year retrospective study","authors":"A. Ghimire, P. Pant, Nilam Subedi, S. R. Pant","doi":"10.3126/GMJ.V1I1.22402","DOIUrl":"https://doi.org/10.3126/GMJ.V1I1.22402","url":null,"abstract":"Background: The use of laparoscopic surgery in modern gynecology has led to faster recovery, lesser hospital stay, and fewer complications. In this study, we aim to analyze the current trends in laparoscopic surgery, its indications, type of procedure and associated complications. \u0000Method: This is a retrospective study done in Grande International Hospital. All patients who underwent laparoscopic surgery over a duration of 5 years from July 2013 to June 2018 were analyzed. \u0000Result: There were a total of 419 laparoscopic surgeries (74 diagnostic, 345 therapeutic) performed. The most common age group of patients for diagnostic laparoscopy was 25-34 years and for therapeutic was 45-54 years. Therapeutic surgery was mostly performed for ovarian cyst (144, 41.74%). There were a total of 152 (44.06%) laparoscopic hysterectomies performed. Complications which occurred during the surgery were insignificant (p<0.01). \u0000Conclusion: Laparoscopic surgery has become the most common procedure for gynecological procedures over the years.","PeriodicalId":314361,"journal":{"name":"Grande Medical Journal","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128750039","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Neuroendoscopic lavage and continuous drainage of ventricles: Treatment of pyocephalus in a newborn","authors":"Rama Joshi, R. Adhikari, Amit Thapa","doi":"10.3126/GMJ.V1I1.22415","DOIUrl":"https://doi.org/10.3126/GMJ.V1I1.22415","url":null,"abstract":"Pyocephalus/Cerebral ventricular empyema is a serious life threatening complication of acute pyogenic meningitis. The primary treatment of ventriculitis is administration of antibiotics. With recent advances, neuroendoscopic lavage (NEL) of ventricles through direct visualization has helped save lives when multipronged approaches including intravenous (IV) antibiotics, intrathecal antibiotics and continuous drainage of cerebrospinal fluid (CSF) fails. \u0000We report a case of a 23-day old neonate who developed pyocephalus as a complication of pyogenic meningitis. He did not respond favorably to initial IV antibiotic treatment for two weeks. NEL of ventricles was performed. Thick pus/flakes inside the ventricles had caused obstructive hydrocephalus. Continuous CSF drainage was done through strategically placed multiple external ventricular drains. Interval ventriculo-peritoneal shunt was done bilaterally after the CSF was macroscopically/ microscopically clear of visible debris, and sterile. Microbiological and clinical cure was achieved and the child survived and is thriving well at last follow-up at the age of 6 months.","PeriodicalId":314361,"journal":{"name":"Grande Medical Journal","volume":"62 5","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"113968074","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}