ABSTRACT Intestinal cestode(tapeworm ) is characterized by multisegmented, scolex, and absence of digestive tracts as appears in our segments, we reported nine segments of tape worm with,scolex,neck,13-17 uterus branch, and scorpion like tail.

We describe a 63-year-old male with systemic AL amyloidosis with cardiac, renal, and liver involvement. After 4 courses of CyBorD, mobilization with G-CSF was initiated and CART was simultaneously performed for fluid retention. Anasarca gradually disappeared and he underwent autologous hematopoietic stem cell transplantation.

We present a case report of an immunocompetent African young man who presented with persistent chest pain and fever, and was diagnosed with EPTB following chest CT scan, pleural biopsy histopathology examination and Ziehl-Neelsen (ZN) staining, and pleural fluid gene Expert studies.

Necrotizing pneumonia (NP) is a severe form of lung disease with a high mortality rate. Although NP generally occurs as a complication in community-acquired pneumonia, our case illustrates that NP can occur as a secondary infection even if the clinical course of COVID-19 pneumonia is favorable, particularly in intubated patients.

This work aimed to report a rare case of a non-calcifying Pindborg Tumor involving the right mandible. The absence of calcifications in the calcifying epithelial odontogenic tumor presents a diagnostic challenge and prognostic implications. A literature review of the sixteen reported clinical cases of this scarce variant was performed.

A document by Ayah El-Qaderi. Click on the document to view its contents.

A 67-year-old Japanese man was referred to us with numerous papules and nodules. Examination revealed i) IgM-monoclonal proteinemia, ii) amyloid protein deposition around vessels in the dermis and subcutis, and iii) lymphoplasma cells into bone marrow. This report shows that Waldenström’s macroglobulinemia causes papules/nodules through the development of amyloidosis.

We present a case of a second-born breastfed infant presenting with zinc deficiency whose mother was found to have a novel heterozygous mutation in SLC30A2. A previous baby did not have manifestations of zinc deficiency but the mother had taken a proton pump inhibitor during the second pregnancy.

Here, we report a case of endovascular treatment in which optical frequency domain imaging (OFDI) evaluated the scoring balloon elements shift when three inflations without shaft rotation performed with a scoring balloon.

Takayasu arteritis is a granulomatous inflammation of the aorta and its major branches.Can present as an isolated, atypical,and/or catastrophic disease.The disease has been reported around the world, although it appears to be more prevalent in Asians.We report case of a 29-year-old pregnant lady presented with TA.

Presentation of High Altitude Pulmonary Edema (HAPE) in accordance with its usual natural history is a diagnostic clue. In resource-limited settings, distinguishing HAPE from other respiratory illnesses is challenging; especially when the presentation deviates from the natural history. Here we have discussed those three rare presentations of HAPE at 4371m.

Disseminated adenovirus infections in patients who received chemotherapy alone for lymphoma are extremely rare, however, should be included in differential diagnosis for those who received T cell suppressive agents. We report a fatal case of disseminated adenovirus disease in a patient who had received chemotherapy and presented with hypoxia

Brugada syndrome is a genetic arrhythmia syndrome characterized by a coved type of ST segment elevation in the ECG.The patients are usually asymptomatic, with unmasking of the disease under certain conditions.We are reporting the case of such a patient who was diagnosed during an attack of dengue fever

Trapezium fracture is a rare condition that goes undetected and exposes to long-term comorbidities : chronic pain and rhizartrosis. In presence of suggestive clinical presentation with a normal radiograph, CT scan should be considered. Therapeutic guidelines are not well established due to the lack of series reported in the literature.

Herpes Simplex Encephalitis is the most common cause of infectious encephalitis. Our case is of a 75-year-old woman who presented with dysuria and altered mental status. Our case addresses the difficulties in diagnosis and highlights the importance of early recognition of HSE and its associated neurological sequelae.

Myopathy-related symptoms are rare manifestations of hypothyroidism. Clinicians should consider hypothyroid myopathy as one of possible diagnosis for patients with proximal weaknesses. We report a 34-year-old woman, presenting with a new atypical musculoskeletal manifestation of hypothyroidism mimicking polymyositis.

Alveolar bone exostoses (ABE) are benign localized convex outgrowths of buccal or lingual bone from the cortical plate, often known as buttress bone development. Our review and case series shows ABE following orthodontic treatment. If self-remission fails after orthodontic forces are removed, we have shown surgical methods to correct ABE

Several approaches can correct pseudo Class III anterior crossbite. 2x4 appliance, compressed open coil springs, Class III elastics, etc. All cause either soft tissue lacerations, smile line flattening or upper incisor overproclination.This paper describes a novel method to tip lower incisors into a normal overjet without compromising the upper dentition