Neuroendocrine neoplasms of the orbit: report of three cases and a literature review.

Neuroendocrine neoplasms (NENs) originate from neuroendocrine cells, and mainly occur in the gastrointestinal tract and lungs, rarely occurring in the orbit. Here, the clinicopathologic factors, treatments and prognosis of three cases of orbital NENs are described. The mean age of the three patients (two females and one male) was 59 years. Two cases exhibited ocular symptoms, including unilateral proptosis and eyelid mass, while the third case presented systemic symptoms exhibited as Cushing's syndrome. The tumours were surgically resected in all three patients. Immunohistochemistry assays revealed positive expression for pan cytokeratin and epithelial membrane antigen in all cases. Additionally, neural cell adhesion molecule 1 (also known as CD56) and synaptophysin were positive in two cases. The pathological diagnosis for case 1 and 2 was 'neuroendocrine carcinoma' and both patients died three months after diagnosis. Case 3 was diagnosed with a neuroendocrine tumour and the symptoms of Cushing's syndrome gradually improved following surgery. In addition, no recurrence was observed during the four-year follow-up period. These cases demonstrate that orbital neuroendocrine tumours show different clinical manifestations due to the different types. Pathology may clarify the diagnosis, classification and grading, and provide a reference value for treatment and prognosis.

Erdheim-Chester disease with bilateral orbital masses and multi-systemic symptoms: two case reports.

BACKGROUND: Erdheim-Chester disease (ECD) is a rare histiocytic disorder characterized by multisystem xanthogranulomatous infiltration by lipid-laden histiocytes. We report two cases of ECD involving the orbit and describe their clinicopathologic factors, treatments, and prognosis. One was a rare case of ECD complicated with primary thrombocytosis. CASE PRESENTATION: This study describes two patients with bilateral orbital ECD. Both presented with proptosis and visual loss; imaging findings showed bilateral intraorbital masses. Both had different degrees of systemic symptoms (pleural effusion, pericardial effusion, ascites, and heart failure) before the ocular symptoms and did not find the cause before ophthalmic tumor resection and pathological biopsy. The diagnosis of ECD was confirmed after pathological biopsy and detection of BRAFV600E mutation. Patient 2 also with primary thrombocytosis and had a CALR mutation as well as the BRAFV600E mutation. Both patients were recommended to receive targeted therapy. Patient 1 refused targeted therapy for financial reasons and was discharged after local radiotherapy only. The patient had no light perception in either eye and no improvement in systemic symptoms. Patient 2 began targeted treatment after diagnosis and reached the discharge criteria 2 weeks later. He is in good condition at present, but unfortunately, his eyesight has not improved because of the irreversible damage to his visual function. CONCLUSION: ECD is easily misdiagnosed and missed because of its rarity and diverse clinical manifestations. Orbital involvement is common in ECD, and surgery is the most frequently employed approach. Despite the surgical resection is not curative, its significance lies in biopsy to establish diagnosis and/or surgical debulking to relieve mass effect, minimizing further impairment of visual function. Targeted therapy is the most effective treatment for patients with a positive BRAF mutation gene. Evaluation of a concomitant myeloid neoplasm is also critical before initiating targeted therapies for refractory ECD.

Hydrogen-Bond-Connected 2D Zn-LMOF with Fluorescent Sensing for Inorganic Pollutants and Nitro Aromatic Explosives in the Aqueous Phase.

Herein, a novel luminescent Zn-LMOF, JLU-MOF109 ([Zn(PBBA)(H2O)]·3DMF·2H2O, PBBA = 4,4'-(2,6-pyrazinediyl)bis[benzoic acid], DMF = N,N-dimethylformamide), was successfully synthesized under solvothermal conditions. Zinc ions are connected by PBBA ligands to form two-dimensional (2D) layers, and the layers are further propped up through hydrogen-bonding interactions. JLU-MOF109 exhibits good sensitivity to inorganic pollutants, Fe3+ and Cr2O72-, as well as nitro aromatic explosives, 2,4,6-trinitrophenol and 2,4-dinitrophenol. JLU-MOF109 exhibits high Ksv (at 104 M-1 level) and low limit of detection values (∼10-6 mol/L) for the abovementioned hazardous pollutants, which is better than a majority of previously reported MOF-based fluorescent sensors. With good stability in the aqueous phase, JLU-MOF109 can serve as a promising chemical sensor for pollutant detection in wastewater.

Unique Fluorescence Turn-On and Turn-Off-On Responses to Acids by a Carbazole-Based Metal-Organic Framework and Theoretical Studies.

Distinct from predominately known fluorescence quenching (turn-off) detection, turn-on response to hazardous substances by luminescent metal-organic frameworks (LMOFs) could greatly avoid signal loss and susceptibility to environmental stimulus. However, such detection rarely occurs and lacks theoretical elucidations. Here, we present the first example of unique turn-on and unprecedented turn-off-on responses to a variety of acids by a stable 12-connected hexanuclear Y(III)-cluster-based LMOF material─JLU-MOF111, featuring the nondefault pcu topology. Benefiting from the "pocket" structures formed by the carbazole-containing ligands, JLU-MOF111 can sense multiple inorganic and organic acids via different degrees of fluorescence turn-on behaviors. Particularly, turn-on sensing of HNO3, HCl, HBr, and TFA is hypersensitive with LODs as low as the ppb level. Theoretical calculations confirm weak interactions in acid-ligand complexes, which lead to constrained rotations of benzene moieties of the ligands when the complexes decay from excited states. These account for the turn-on response through reduced nonradiative energy consumption that competes with emissive decay. The turn-off-on response to 4-NBA and 3,5-DNBA involves an excited-state electron transfer process that dominates the turn-off stage and prohibited nonradiative decay that competes with the intrinsic emission of the ligand and dominates the turn-on stage. This work has a guiding significance for the full-scale understanding of turn-on and turn-off-on sensing performance in LMOF materials and beyond.

A Stable Y(III)-Based Amide-Functionalized Metal-Organic Framework for Propane/Methane Separation and Knoevenagel Condensation.

Here, a Y(III)-based metal-organic framework, JLU-MOF112 {[Y3(µ3-O)2(µ3-OH)(H2O)2(BTCTBA)2]·2[(CH3)2NH2]·5DMF·C6H5Cl·4H2O}, has been successfully synthesized under solvothermal conditions. JLU-MOF112 was constructed with amide-functionalized tricarboxylate ligands and Y(III)-based infinite chains, where the Y3 repeating units are arranged in a trans order. The overall framework could be viewed as a novel (3,5)-connected net with two types of channels along the [100] and [010] directions. JLU-MOF112 possesses a large BET surface area (1553 m2 g-1), a permanent pore volume (0.67 cm3 g-1), and outstanding thermal and chemical stability, which give JLU-MOF112 potential for the purification of natural gas, especially the equimolar separation of C3H8/CH4 with a high selectivity of 176. In addition, benefiting from the amide functional groups as Brønsted basic sites and the exposure of open metal sites as Lewis acid sites after activation, JLU-MOF112 can serve as a high-efficiency heterogeneous catalyst for Knoevenagel condensation by the reactions of malononitrile with benzaldehyde (yield of 98%, turnover number of 392, and turnover frequency of 3.27 min-1) and diverse aldehyde compounds. A rational mechanism was put forward that the Knoevenagel condensation was catalyzed by the synergistic effect of the Lewis acid sites and Brønsted basic sites, engendering the polarization of the carbonyl groups and the deprotonation of the methylene groups for nucleophilic attack.

Structural Regulation and Light Hydrocarbon Adsorption/Separation of Three Zirconium-Organic Frameworks Based on Different V-Shaped Ligands.

On the basis of different V-shaped ligands, three zirconium-organic frameworks (JLU-Liu45, Zr-SDBA, and Zr-OBBA) have been successfully constructed. By regulating spatial configuration and functional groups of organic ligands, these as-synthesized Zr-MOFs (MOF = metal-organic framework) display distinct structures and different light hydrocarbon adsorption/separation capabilities. JLU-Liu45, with a double-walled interpenetrated 3D primitive cubic (pcu) framework, exhibits good gas-adsorption capacity but not prominent selective separation ability. Through regulating sizes and torsion angles of the organic ligands, Zr-SDBA possesses a 2D square lattice (sql) network, while Zr-OBBA displays a non-interpenetrated 3D pcu framework. Furthermore, by regulating functional groups on the ligands, Zr-SDBA shows prominent C2H2 uptake (101.2 cm3·g-1) and the best C2H2/CH4 selectivity (230.5, 1:1) among the three Zr-MOFs, and Zr-OBBA shows a significant C3H8/CH4 selectivity (105.6, 1:1). This work demonstrates the feasibility of structural regulation for MOF materials in the light hydrocarbon adsorption/separation field.