In-situ synthesized ZIF-67 graphene oxide (ZIF-67/GO) nanocomposite for efficient individual and simultaneous detection of heavy metal ions.

Heavy metals are ubiquitous in water bodies as a result of anthropogenic activities and over time they accumulate in body thus posing serious health problems. Therefore, it is essential to improve sensing performance, for determination of heavy metal ions (HMIs), of electrochemical sensors. In this work, cobalt-derived MOF (ZIF-67) was in-situ synthesized and incorporated onto the surface of graphene oxide (GO) by simple sonication method. The prepared material (ZIF-67/GO) was characterized by FTIR, XRD, SEM, and Raman spectroscopy. Afterwards, a sensing platform was made by drop-casting synthesized composite onto glassy carbon electrode for individual and simultaneous detection of heavy metal ions pollutants (Hg2+, Zn2+, Pb2+, and Cr3+) with estimated detection limits of 2 nM, 1 nM, 5 nM, and 0.6 nM, respectively, when determined simultaneously, that are below the permissible limit by World Health Organization. To the best of our knowledge, this is first report of HMIs detection by ZIF-67 incorporated GO sensor which can successfully determine the Hg+2, Zn+2, Pb+2, and Cr+3 ions simultaneously with lower detection limits.

Rare occurrence of pseudomyxoma peritonei (PMP) syndrome arising from a malignant transformed ovarian primary mature cystic teratoma treated by cytoreductive surgery and HIPEC: a case report.

BACKGROUND: Pseudomyxoma peritonei (PMP) syndrome is a disease process that typically occurs from ruptured appendiceal mucocele neoplasms. PMP syndrome arising from malignant transformation of an ovarian primary mature cystic teratoma (MCT) is a pathogenesis rarely encountered. CASE PRESENTATION: Herein, we report a 28-year-old patient evaluated and treated for a right ovarian mass and large volume symptomatic abdominopelvic mucinous ascites. Molecular profiling and genetic analysis revealed mutations in ATM, GNAS, and KRAS proteins while IHC demonstrated gastrointestinal-specific staining for CK20, CDX2, CK7, and SATB2. Peritoneal cytology showed paucicellular mucin. Diffuse peritoneal adenomucinosis (DPAM) variant of PMP arising from a ruptured ovarian primary MCT after malignant transformation to a low-grade appendiceal-like mucinous neoplasm was ultimately confirmed. Treatment included staged therapeutic tumor debulking and right salpingo-oophorectomy followed by cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (HIPEC). CONCLUSIONS: Our report builds upon the existing literature supporting this aggressive treatment option reserved for advanced abdominal malignancies utilized in this patient with a rare clinical entity.

Educational Case: Asthma: Clinical Features and Morphologic Findings.

The following fictional case is intended as a learning tool within the Pathology Competencies for Medical Education (PCME), a set of national standards for teaching pathology. These are divided into three basic competencies: Disease Mechanisms and Processes, Organ System Pathology, and Diagnostic Medicine and Therapeutic Pathology. For additional information, and a full list of learning objectives for all three competencies, see http://journals.sagepub.com/doi/10.1177/2374289517715040.1.

Educational Case: Myocardial Infarction: Histopathology and Timing of Changes.

The following fictional case is intended as a learning tool within the Pathology Competencies for Medical Education (PCME), a set of national standards for teaching pathology. These are divided into three basic competencies: Disease Mechanisms and Processes, Organ System Pathology, and Diagnostic Medicine and Therapeutic Pathology. For additional information, and a full list of learning objectives for all three competencies, see http://journals.sagepub.com/doi/10.1177/2374289517715040.1.