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Myeloid sarcoma presenting as a colon polyp and harbinger of chronic myelogenous leukemia
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作者 Robert Rogers Mark Ettel +3 位作者 Margaret Cho Alexander Chan Xiao-Jun Wu Antonio G Neto 《World Journal of Gastrointestinal Oncology》 SCIE CAS 2016年第3期321-325,共5页
Myeloid sarcoma, also known as granulocytic sarcoma or chloroma is an unusual accumulation of malignant myeloid precursor cells in an extramedullary site, which disrupts the normal architecture of the involved tissue.... Myeloid sarcoma, also known as granulocytic sarcoma or chloroma is an unusual accumulation of malignant myeloid precursor cells in an extramedullary site, which disrupts the normal architecture of the involved tissue. It is known to occur more commonly in patients with acute myelogenous leukemia and less commonly in those with myelodysplastic syndrome and myeloproliferative neoplasm, such as chronic myelogenous leukemia. The most common sites of involvement include bone, skin and lymph nodes. However, rare cases have been reported in the gastrointestinal tract, genitourinary tract, or breast. Most commonly, a neoplastic extramedullary proliferation of myeloid precursors in a patient would have systemic involvement of a myeloid neoplasm, including in the bone marrow and peripheral blood. Infrequently, extramedullary disease may be the only site of involvement. It may also occur as a localized antecedent to more generalized disease or as a site of recurrence. Herein, we present the first case in the English literature of a patient presenting with an isolated site of myeloid sarcoma arising in the form of a colonic polyp which, after subsequent bone marrow biopsy, was found to be a harbinger of chronic myelogenous leukemia. 展开更多
关键词 MYELOID SARCOMA Granulocytic SARCOMA CHLOROMA Chronic MYELOGENOUS LEUKEMIA
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Synovial osteochondromatosis of the temporomandibular joint: A case report
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作者 Nahir Romero Collin F Mulcahy +3 位作者 Stephanie Barak Muhammed F Shand Christopher D Badger Arjun S Joshi 《World Journal of Otorhinolaryngology》 2019年第2期12-18,共7页
BACKGROUND Synovial osteochondromatosis is a rare but benign condition that can result in significant impairment of joint functionality.This case report documents an uncommon presentation of this disorder occurring wi... BACKGROUND Synovial osteochondromatosis is a rare but benign condition that can result in significant impairment of joint functionality.This case report documents an uncommon presentation of this disorder occurring within the temporomandibular joint,causing the patient significant pain,trismus,and difficulty with daily activities such as eating and speaking.A review of the literature including disease mechanisms and previously documented cases is included to provide comprehensive background for clinical decision-making.CASE SUMMARY A 48-year-old male patient presented with a 3-mo history of trismus,crepitus with jaw movement and significant pain while chewing.Physical examination revealed a firm mass and tenderness to palpation at the right temporomandibular joint.Further workup revealed a bilobed mass extending into the joint space as well as significant bony erosion of the glenoid fossa.The patient underwent mass excision with joint reconstruction and pathology revealed synovial osteochondromatosis.The patient reported significant improvement in his symptoms postoperatively.CONCLUSION This report outlines the investigative approach and treatment course of synovial osteochondromatosis.The positive outcome following surgical intervention in this case emphasizes the importance of interdisciplinary collaboration and the potential for improvement in quality of life of this patient population. 展开更多
关键词 OSTEOCHONDROMATOSIS Temporomandibular joint MANDIBLE RESECTION Case report
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A novel indocyanine green-based fluorescent marker for guiding surgical tumor resection 被引量:1
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作者 Jiawei Ge Justin D.Opfermann +6 位作者 Hamed Saeidi Katherine A.Huenerberg Christopher D.Badger Jaepyeong Cha Martin J.Schnermann Arjun S.Joshi Axel Krieger 《Journal of Innovative Optical Health Sciences》 SCIE EI CAS 2021年第3期77-87,共11页
Surgical tumor resection is a common approach to cancer treatment.India Ink tattoos are widely used to aid tumor resection by localizing and mapping the tumor edge at the surface.However,India Ink tattoos are easily o... Surgical tumor resection is a common approach to cancer treatment.India Ink tattoos are widely used to aid tumor resection by localizing and mapping the tumor edge at the surface.However,India Ink tattoos are easily obscured during electrosurgical resection,and fade in intensity over time.In this work,a novel near-infrared(NIR)fluorescent marker is introduced as an alternative.The NIR marker was made by mixing indocyanine green(ICG),biocompatible cyanoacrylate,and acetone.The marking strategy was evaluated in a chronic ex vivo feasibility study using porcine tissues,followed by a chronic in vivo mouse study while compared with India Ink.In both studies,signal-to-noise(SNR)ratios and dimensions of the NIR markers and/or India Ink over the study period were calculated and reported.Electrocautery was performed on the last day of the mouse study after mice were euthanized,and SNR ratios and dimensions were quantified and compared.Biopsy was performed at all injection sites and slides were examined by a pathologist.The proposed NIR marker achieved(i)consistent visibility in the 26-day feasibility study and(ii)improved durability,visibility,and biocompatibility when compared to traditional India Ink over the six-week period in an in vivo mouse model.These effects persist after electrocautery whereas the India Ink markers were obscured.The use of a NIR fluorescent presurgical marking strategy has the potential for intraoperative tracking during long-term treatment protocols. 展开更多
关键词 Near-infrared fluorescent marker surgical tumor resection fluorescence-guided sur-gery ELECTROSURGERY India ink
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