Clinics and Practice http://www.clinicsandpractice.org/index.php/cp <p><strong>Clinics and Practice</strong>&nbsp;[ISSN 2039-7283] is a peer-reviewed, Open Access, online-only journal that publishes both&nbsp;<em>brief reports</em>&nbsp;and&nbsp;<em>case reports</em>&nbsp;in all areas of clinical medicine. Our journal would welcome any interesting description of patients, procedures and treatment in any condition or disease useful for healthcare professionals.<br><br></p> en-US <p>PAGEPress has chosen to apply the&nbsp;<a href="http://creativecommons.org/licenses/by-nc/4.0/" target="_blank" rel="noopener">Creative Commons Attribution NonCommercial 4.0 International License</a>&nbsp;(CC BY-NC 4.0) to all manuscripts to be published.&nbsp;<br><br>An Open Access Publication is one that meets the following two conditions:<br><br>1. The author(s) and copyright holder(s) grant(s) to all users a free, irrevocable, worldwide, perpetual right of access to, and a license to copy, use, distribute, transmit and display the work publicly and to make and distribute derivative works, in any digital medium for any responsible purpose, subject to proper attribution of authorship, as well as the right to make small numbers of printed copies for their personal use.<br>2. A complete version of the work and all supplemental materials, including a copy of the permission as stated above, in a suitable standard electronic format is deposited immediately upon initial publication in at least one online repository that is supported by an academic institution, scholarly society, government agency, or other well-established organization that seeks to enable open access, unrestricted distribution, interoperability, and long-term archiving.<br><br>Authors who publish with this journal agree to the following terms: 1. Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal. 2. Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal. 3. Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work.</p> paola.granata@pagepress.org (Paola Granata) tiziano.taccini@pagepress.org (Tiziano Taccini) Wed, 28 Mar 2018 17:31:56 +0200 OJS 3.1.1.0 http://blogs.law.harvard.edu/tech/rss 60 Systemic lupus erythematosus flare up as acute spinal subarachnoid hemorrhage with bilateral lower limb paralysis http://www.clinicsandpractice.org/index.php/cp/article/view/1069 <p>Subarachnoid hemorrhage (SAH) is an uncommon complication of systemic lupus erythematosus (SLE). Solitary association of fatal spinal SAH as a complication of SLE, has not been encountered much in literature although coexisting acute cerebral and spinal SAH have been associated with SLE. We present a 39-year old female with initial diagnosis of SLE eight years ago who suddenly developed a productive cough, acute abdomen and paralysis of the lower limbs. Magnetic resonance imaging of the spine revealed thoracic spinal SAH with varying degrees of thoracic spinal cord compression. The hemorrhage was total evacuated via surgery. She regained normal function of her lower limbers after the operation with no further neurological complications. One of the rare but fatal complications of SLE is solitary spinal SAH without cranial involvement. The best and most appropriate management of this kind of presentation is surgical decompression of the hematoma with total hemostasis. The cause of hemorrhage should be identified intra-operatively and treated appropriately.</p> Xiang Yang, Seidu A. Richard, Jiagang Liu, Siqing Huang ##submission.copyrightStatement## http://creativecommons.org/licenses/by-nc/4.0 http://www.clinicsandpractice.org/index.php/cp/article/view/1069 Thu, 10 May 2018 00:00:00 +0200 Revisiting transthyretin related cardiac amyloidosis: Case report and review of literature http://www.clinicsandpractice.org/index.php/cp/article/view/1054 <p>Amyloidosis is a complex group of disorders that can involve many organs and cause their dysfunction. Cardiac involvement indicates worse prognosis and influences treatment strategies. Cardiac amyloidosis is an under-diagnosed entity and high index of clinical suspicion and careful interpretation of basic diagnostic tools such as electrocardiogram and echocardiography is needed for early detection. Congestive heart failure due to restrictive pattern and/or conduction system abnormality, in absence of coronary artery disease should raise suspicion. We present a case of transthyretin related cardiac amyloidosis and discuss the key clinical and diagnostic findings along with review of existing literature regarding its management and outcomes.</p> Munish Sharma, Eduard Koman, Gary S. Ledley, Sung-Hae Cho ##submission.copyrightStatement## http://creativecommons.org/licenses/by-nc/4.0 http://www.clinicsandpractice.org/index.php/cp/article/view/1054 Wed, 16 May 2018 00:00:00 +0200 The frequency of clinical manifestations of hypophosphatemic rickets in patients with therapeutic strategies http://www.clinicsandpractice.org/index.php/cp/article/view/1072 <p>The aim of this study was to evaluate the frequency of clinical manifestations of various types of rickets in patients could be effective in therapeutic strategies. A total of eleven child patients (7 females and 4 males) were included in the present study. The patients were admitted to the hospital with hypophosphatemic rickets. In our study, the age at the time of diagnosis ranged from 1 to15 years. Mean age of first presentations at final diagnosis was determined to be 5.5 an 2 years, respectively. Five patients out of 11 patients had showed significant history of vitamin D3 resistance. Family history of similar skeletal problems was reported to be positive in six patients. Furthermore, there were seven relative marriages in parents. Mean value of Gomez index has been revealed as 64%. Mean serum phosphate level was detected as 2.9 mg/dL, that this level in males (2.2 mg/dL) was significantly less than females (3.4 mg/dL) (P=0.5). Mean serum alkaline phosphatase activity was reached 913 IU/L. Alkaline phosphatase activity in women (1075 IU/L) was significantly lower than that of men (750 IU/L), (P=0.5). Definitive treatment with oral phosphate and vitamin D3 can prevent complications of the disease and the side effects of unconventional treatments.</p> Leila Kanafi Vahed, Afshin Arianpur, Mohammad Esmaeili ##submission.copyrightStatement## http://creativecommons.org/licenses/by-nc/4.0 http://www.clinicsandpractice.org/index.php/cp/article/view/1072 Thu, 10 May 2018 00:00:00 +0200 Misleading hepatitis B serology following Rho (D) immune globulin (human) injection and influenza vaccine http://www.clinicsandpractice.org/index.php/cp/article/view/1037 <p>Having a hepatitis B surface antibody (HBsAb) titre of more than 10 mIU/mL after hepatitis B vaccination is generally considered to confer immunity to hepatitis B. This case report discusses an unusual case of a false positive hepatitis B core total antibody (HBcAb) following administration of either Rho (D) immune globulin (Human) injection or influenza vaccine in a patriuent who was previously immunised against hepatitis B.</p> Xuanxuan Chen ##submission.copyrightStatement## http://creativecommons.org/licenses/by-nc/4.0 http://www.clinicsandpractice.org/index.php/cp/article/view/1037 Wed, 21 Mar 2018 11:28:30 +0100 A case of scarred uterine rupture at 11 weeks of gestation having a uterine scar places induced by in vitro fertilization-embryo transfer http://www.clinicsandpractice.org/index.php/cp/article/view/1038 <p>Having a uterine scar places a woman at increased risk of complications, such as Cesarean scar pregnancy (CSP), uterine rupture, placenta previa, and placenta accreta, in subsequent pregnancies. We report a case of uterine rupture at 11 weeks of gestation in a woman with a previous Cesarean section. A 43-year-old woman with a history of abdominal myomectomy and Cesarean section had her pregnancy induced by <em>in vitro</em> fertilization with donor eggs. The exact location of the gestational sac was identified on her first day of hospitalization, and her pregnancy was suspected to be a CSP. The following day, the patient complained of sudden lower abdominal pain. A uterine scar rupture was diagnosed, and an emergency surgery was required. It may be that first-trimester screening could allow the early recognition of patients at risk for these perinatal complications.</p> Akiko Takashima, Naoki Takeshita, Toshihiko Kinoshita ##submission.copyrightStatement## http://creativecommons.org/licenses/by-nc/4.0 http://www.clinicsandpractice.org/index.php/cp/article/view/1038 Thu, 10 May 2018 18:08:11 +0200 Early prenatal diagnosis of parapagus conjoined twins http://www.clinicsandpractice.org/index.php/cp/article/view/1039 Conjoined twinning occurs in 1/100 of monozygotic twins, 1/50,000 gestations and 1/250,000 live births. It is the consequence of a division event at the primitive streak stage of the human embryonic development, about 13-14 days after fertilisation, in monochorionic monoamniotic gestations. A healthy pregnant woman, Gravida 2 Para 1, was admitted into our Fetal Medicine Unit to perform the first trimester ultrasound. A diagnosis of conjoined parapagus twinning based on ultrasound features was made at 11 weeks of gestation, and the couple decided to terminate the pregnancy. The ultrasound showed two independent skulls and hearts, a shared spine below the thoracic level, and a shared stomach. The pathological findings were slightly different, showing two independent stomachs draining into a common duodenum. The karyotype was 46 XY. Early prenatal ultrasound may provide a window to counsel the family and to offer an early termination of pregnancy. Ângela Melo, Rita Dinis, António Portugal, Ana Isabel Sousa, Isabel Cerveira ##submission.copyrightStatement## http://creativecommons.org/licenses/by-nc/4.0 http://www.clinicsandpractice.org/index.php/cp/article/view/1039 Wed, 28 Mar 2018 09:31:45 +0200 Rectal leiomyoma, a rare entity http://www.clinicsandpractice.org/index.php/cp/article/view/1053 Rectal tumors are often encountered as an incidental finding on screening colonoscopy. As per the World Health Organization, they are categorized according to their histologic appearance. These include epithelial tumors, mesenchymal tumors and lymphomas. Of interest, in our case, are mesenchymal tumors. These are sub-classified into leiomyomas and gastrointestinal stromal tumors. Our case is a 33-year old male who was diagnosed with a rectal leiomyoma. The uncommon incidence and subsequent management of a rectal leiomyoma in a male, make this case worthy for literature review. Tagore Sunkara, Eric Omar Then, Andrea Culliford, Vinaya Gaduputi ##submission.copyrightStatement## http://creativecommons.org/licenses/by-nc/4.0 http://www.clinicsandpractice.org/index.php/cp/article/view/1053 Wed, 21 Mar 2018 10:38:21 +0100