Case Report

1. Abstract 1.1. Background: Intrahepatic cholestasis of pregnancy is a reversible cholestasis typically beginning in the second or third trimester and associated with increased rates of stillbirth, preterm birth, fetal asphyxia, and neonatal care unit admission. The etiology of adverse outcomes in gestational cholestasis seems related to maternal bile acids levels, but recommendations for management, […]

1. Preamble Kimura’s disease is a benign rare inflammatory disorder of unknown aetiology which might mimic neoplastic’s lesion. Epidemiologically this condition, affects young Asian males. Early diagnosis of kimura’s disease may spare the patient from unnecessary invasive diagnostic procedure (surgery-biopsy).

1. Abstract Chediak-Higashi syndrome is a rare autosomal recessive immunodeficiency associated with congenital mutations in the lysosomal trafficking regulator gene (CHS1/LYST).

1. Abstract Histopathology of skin biopsies is invaluable for the diagnosis of skin conditions. However, it is an elaborate and time-consuming procedure whose diagnostic yield depends on the experience of highly trained experts.

Abstract 1.1. Background: Mycoplasma pneumonia is a common community pathogen associated with lower respiratory tract infection.

1. Abstract Stercoral perforation is a rarely suspected life-threatening condition due to an extensive and widespread contamination of the peritoneal cavity with fecal matter. Various pathological conditions associated with acute abdomen and suspected intestinal perforation are usually linked to complicated diverticulitis due to foreign objects.

1. Summary Eosinophilic gastrointestinal diseases (EGIDs) are rare, im- mune-mediated disorders characterized by eosinophilic infiltra- tion of one or more areas of the gastrointestinal (GI) tract, various gastrointestinal symptoms depending on the affected tract region, as well as depth and extent of eosinophilic infiltration, and the absence of other known causes of eosinophilia.

1. Abstract Pyothorax-associated lymphoma (PAL) is a rare disease with variations in endemic prevalence. PAL arising from a posttraumatic empyema are a rare occurrence. Here, we report a case of Epstein- Barr virus (EBV)-positive PAL arising from a posttraumatic empyemae. A male patient, 83 years old. Twenty years earlier, the patient fell from a height,

1. Abstract Rosai-Dorfman-Destombes disease is a very rare benign disorder of histiocyte proliferation with unknown etiology. We report the case of a 41 years old man diagnose with this disease, having had long standing cervical lymphadenopathy increasing in size. This case is presented given the difficulty in diagnosis and surgical management on skin involvement.

1. Abstract A rare cause of foot pain is described in which the diagnostic accuracy of the MRI proved vital in pinpointing the location of the aetiology and subsequently in corrective surgery.