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  • ISSN: 2373-9819
    Body Stalk Anomaly in One of the Dichorionic Diamniotic Twins Following In vitro Fertilization and Embryo Transfer
    Authors: Krishna GR, Abdul Haium Abdul Alim, Kenneth Chang TE, Edwin Thia WH and Bhavani Sriram
    Abstract: Body stalk anomaly/Limb body wall complex (BSA/LBWC) is a sporadic, rare and severe congenital anomaly with a poor prognosis.
    A Rare Cause of Hip Pain: Primary Tuberculous Psoas Abscess. Case Report
    Authors: Carlos Cano, Roberto G. Alconada, German Borobio, Diego A. Rendon, Laura Alonso, David Pescador and Juan F. Blanco
    Abstract: Tuberculous abscesses in the iliopsoas muscle are usually secondary to Potts disease or spinal tuberculosis. Another possibility is direct extension from nearby structures or hematogenous spread from a distant focus.
    Latest Articles
    Case Report
    Noman Shahzad* and Abdul Rehman
    Laparoscopic Cholecystectomy was performed in a morbidly obese patient (BMI 44.35) who presented with recurrent attacks of biliary colic.
    Carolina Fonseca* and Aziz Mohamad
    Collision tumor consisting of medullary thyroid carcinoma and papillary thyroid carcinoma is an extremely rare occurrence 3. We report a case of an 89 year old female diagnosed with uncommon collision tumor of the thyroid based on cytological evaluation of a fine needle aspiration specimen.
    Stella Cortes Verdasca*, Domingas Pereira, and Jose Vaz
    Buerger's disease or thromboangiitis obliterans is an inflammatory, non-atherosclerotic process that affects small and medium-sized vessels and nerves at the extremities. It is manifested by pain and claudication of the fingers, evolving into necrosis and ulceration. Amputation is a reality for many patients.
    Buerger's disease is rare, and the pathophysiological mechanisms that trigger it are not clear. However, there has been good progress in understanding the pathogenesis of the disease and there is a strong association with smoking, immunity, disorders of coagulation and heredity. This is a clear example that exposure to tobacco contributes to the onset and worsening of the disease. Smoking cessation and vasodilator therapy appear to be the best therapeutic strategy.
    Krishna Prasad K, Rahul Singh R*, Amal Abraham, Padmalakshmi, Rami Reddy, Vijay Kumar, and Sreeramulu PN
    Background: Pilonidal sinus is a cavity in the subcutaneous tissue which is lined by granulation tissue contains hair and communicates with the surface by a track line usually by squamous epithelium continuous with the epidermis. It is a disease that most commonly arises in the hair follicles of the natal cleft of the sacrococcygeal area. Incidence is reportedly 26 per 100,000 populations, affecting males four times as often as females and predominantly young adults [1]. In this study we compared minimally invasive crystallized phenol application with modified Limberg flap reconstruction as the treatment strategies for pilonidal sinus in terms of length of hospital stay, rates of recurrence and infection, time taken for wound healing and complication rates.
    Methods: A prospective study in which 22 patients undergoing treatment for pilonidal sinus were studied from December 2015 to November 2017. Block Randomisation applied. Post operative pain, duration of stay in the hospital, development of surgical site infections (SSIs) and other demographic data was analyzed.
    Results: Out of 22 patients undergoing treatment for pilonidal sinus, 11 each were divided into 2 groups with group A, treated with Crystallized phenol application and group B treated with modified Limberg flap reconstruction. Crystallized phenol application is non invasive and patient friendly technique with less duration of stay in hospital and cost effective, only disadvantage is that it has high recurrence rate compared to Flap reconstruction.
    Conclusion: Though there have been various other studies done recruiting patients in a bigger number, this study and the data obtained goes in favor of phenol treatment to be a convenient treatment of choice for pilonidal sinus disease because of its many advantages such as being a minimally invasive procedure, performed under local anesthesia, higher success rate after multiple applications, and decreased length of stay in hospital with minimal surgical scar formation.
    Case Report
    Nemalidinne Keerthi*, Mohan Kumar K, Raghupathi, Prakash M, and Sreeramulu PN
    Breast tuberculosis is a rare manifestation of extra-pulmonary localization of the disease which accounts for less than 0.1% of breast conditions in developed countries, but reaches 3-4% in regions where the disease presents with high incidence. It appears mostly in women of reproductive age. We report a 34 year old lady with right breast lump and axillary lymphadenopathy. Smear for tuberculosis and TB tissue cultures were positive and the histopathology repeatedly showed granulomatous inflammation. Treatment with surgery followed by standard anti tubercular drugs was started once mycobacterium tuberculosis was finally cultured from the excised tissue. This case highlights the difficulty in differentiating culture negative tuberculosis from other causes of chronic granulomatous mastitis and the importance of keeping a high index of clinical suspicion.
    Venkat Reddy Kallem*
    Orofacial clefts are the most common craniofacial malformations and include Cleft Lip with or without associated Cleft Palate [CL/P] or isolated Cleft Palate. Failure of fusion of median nasal process with maxillary processes and fusion of lateral palatal shelves results in cleft lip and cleft palate respectively. Optimal management of CL/P includes multidisciplinary team comprising of Paediatrician, Plastic Surgeon, Otorhinolaryngologist, Maxillofacial Surgeon, Orthodontist, Speech Therapist, Geneticist, Psychologist and Public Health Nurse. Closure of the lip is usually done around 10-12 weeks of life and cleft palate is repaired before 12 months of age. Various techniques of closure are followed based on the type of the defect. Velopharyngeal insufficiency after cleft palate repair is common and these children should be under follow up and require speech evaluation and speech therapy to have optimum function.
    Constantine Kanakis*, Mohamed S. Aziz, and Stanley J. Oiseth
    Primary pulmonary lymphoma (PPL) is a rare entity. PPL cases of T-cell origin represent a small, even less frequent subset. Only 19 such cases of T-cell PPL have been reported in literature, with none having a history of prior radiation or chemotherapy. Reported here, is a case of primary pulmonary peripheral T-cell lymphoma (PTCL) in a 63-year-old woman with a significant history of breast carcinoma six years prior, treated by wide local excision followed by standard adjunctive chemotherapy and radiation. Despite such rarity, PPL/PTCL should be included in the differential of pulmonary nodules, regardless of the clinical scenario or pretest probabilities. This case highlights the problems in diagnosing this entity, the historical epidemiologic relationship between breast cancer and lymphoma. It also highlights a distinct opportunity to examine errors in medical diagnoses and potential inclusions in future differential diagnoses algorithms.
    Thomas Busch* and Aziz Mohamad
    Amyloidoma is a rare presentation of tissue amyloid deposition usually seen in the respiratory, genitourinary, and gastrointestinal tracts, but has also been reported in the mediastinum, central nervous system, skin, breast, and soft tissue. In this case, a 55-year-old man presented with a 5-cm soft tissue mass in the gluteal region, suggestive of a lipoma. Eventually the mass was found to be an isolated amyloidoma associated with a localized plasmacytoma. Soft-tissue amyloidoma in the absence of systemic amyloidosis or plasma cell dyscrasia in bone marrow is uncommon, and those localized to the extremities are extremely rare.
    Carolina Fonseca*, Lawrence Brookman, Mohamad Aziz, Alicia Heidenreich, and Mario Dervish
    Myoepithelial carcinomas are rare. To the best of our knowledge, this case report accounts for the third report in the English literature of this malignant tumor occurring in the foot. This case is also unique in that the patient was a ten-year-old child who presented with metastasis to inguinal lymph node. This case highlights the importance of keeping myoepithelial carcinoma in the differential list when diagnosing soft tissue tumors.
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