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Post-polypectomy coagulation syndrome: a tricky to diagnose hot snare problem that can be eliminated thanks to cold snare revolution. 息肉切除术后凝血综合征:一个棘手的诊断热陷阱问题,可以消除由于冷陷阱革命。
Archive of clinical cases Pub Date : 2022-01-01 DOI: 10.22551/2022.37.0904.10226
Maria Zachou, Konstantinos Pikramenos, Georgios Mpetsios, Efthimia Lalla, Maria Panoutsakou, Konstantinos Varytimiadis, Panayiotis Karantanos
{"title":"Post-polypectomy coagulation syndrome: a tricky to diagnose hot snare problem that can be eliminated thanks to cold snare revolution.","authors":"Maria Zachou,&nbsp;Konstantinos Pikramenos,&nbsp;Georgios Mpetsios,&nbsp;Efthimia Lalla,&nbsp;Maria Panoutsakou,&nbsp;Konstantinos Varytimiadis,&nbsp;Panayiotis Karantanos","doi":"10.22551/2022.37.0904.10226","DOIUrl":"https://doi.org/10.22551/2022.37.0904.10226","url":null,"abstract":"<p><p>Post-polypectomy syndrome or post-polypectomy coagulation syndrome (PPCS) is a rare adverse event of thermal injury caused during hot snare aided, endoscopic mucosal resection of colon polyps. Its diagnosis is tricky as it is commonly misdiagnosed as perforation leading to unnecessary exploratory abdominal surgeries. The authors aim to present an early diagnosed and successfully treated, case of PPCS, and to highlight the difference in the safety profile of two techniques; hot snare versus cold snare polypectomy.</p>","PeriodicalId":72274,"journal":{"name":"Archive of clinical cases","volume":"9 4","pages":"170-172"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/7c/f3/acc-09-04-170.PMC9769077.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10574065","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Accordion sign in COVID 19 related acute myocarditis, an old sign for a novel context? A cardiac magnetic resonance case series report study. COVID - 19相关急性心肌炎的手风琴征:新情况下的旧标志?心脏磁共振病例系列报告研究。
Archive of clinical cases Pub Date : 2022-01-01 DOI: 10.22551/2022.36.0903.10214
Francesco Mangini, Elvira Bruno, Robert W W Biederman, Roberto Del Villano, Roberto Rosato, Eluisa Muscogiuri
{"title":"Accordion sign in COVID 19 related acute myocarditis, an old sign for a novel context? A cardiac magnetic resonance case series report study.","authors":"Francesco Mangini,&nbsp;Elvira Bruno,&nbsp;Robert W W Biederman,&nbsp;Roberto Del Villano,&nbsp;Roberto Rosato,&nbsp;Eluisa Muscogiuri","doi":"10.22551/2022.36.0903.10214","DOIUrl":"https://doi.org/10.22551/2022.36.0903.10214","url":null,"abstract":"<p><strong>Introduction: </strong>The COVID-19 pandemic is related to a higher incidence of myocarditis; we present a case series of seven patients, admitted with COVID-19 related acute myocarditis, evaluated with cardiac magnetic resonance imaging, showing an altered profile of the free wall of the right ventricle, no longer present after six months follow-up.</p><p><strong>Materials and methods: </strong>Seven patients have been evaluated for COVID-19 related acute myocarditis, all patients have been evaluated with cardiac magnetic resonance imaging both in the acute setting and after six months follow-up.</p><p><strong>Results: </strong>In the acute phase, myocarditis was confirmed in keeping with the current diagnostic criteria. In five out of seven cases, the presence of a crinkling profile of the free wall of the right ventricle was observed; at six months follow up, remission in four out of the five cases and a significant reduction in the remaining case, of the previously described findings, was observed.</p><p><strong>Conclusions: </strong>Crinkling appearance in the profile of the free wall of the right ventricle, detectable with cardiac magnetic resonance imaging, might represent a morphological feature present in the acute setting of COVID-19 related myocarditis; several underlying physiopathological mechanisms are conceivable. Further studies are needed to confirm this correlation, define the underlying mechanisms and the prognostic implication related to it. This is the first report in the literature that has considered such findings to the best of our knowledge.</p>","PeriodicalId":72274,"journal":{"name":"Archive of clinical cases","volume":"9 3","pages":"112-116"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/49/b1/acc-09-03-112.PMC9512132.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9286743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Drug induced erythema multiforme of the oral cavity. 药物性口腔多形性红斑。
Archive of clinical cases Pub Date : 2022-01-01 DOI: 10.22551/2022.37.0904.10224
Nalini Aswath, Rajalakshmi Rakshana
{"title":"Drug induced erythema multiforme of the oral cavity.","authors":"Nalini Aswath,&nbsp;Rajalakshmi Rakshana","doi":"10.22551/2022.37.0904.10224","DOIUrl":"https://doi.org/10.22551/2022.37.0904.10224","url":null,"abstract":"<p><p>Drug induced erythema multiforme (EM) is a rare clinical entity which majorly involves the oral cavity. It commonly occurs due to intake of drugs such as NSAID'S, certain antibiotics, and anticonvulsants. It is characterized by rapidly rupturing vesicles leading to ill-defined erosions in the oral cavity and encrusted lip lesions. These lesions are usually difficult to differentiate from other vesiculo bullous and ulcerative lesions which would have a similar presentation and the absence of skin lesions can sometimes lead to misdiagnosis. Drug induced EM has an acute onset and is a self-limiting inflammatory hypersensitivity reaction that causes blistering and ulcerations of the skin and mucous membrane. The lesions heal following the discontinuation of the causative medications. This case report describes a case of drug induced erythema multiforme of the oral cavity that occurred consequent to the intake of Tab.Diclofenac Sodium and Tab.Cephelexin. The patient developed painful, bleeding, burning ulcerations with severe crustations on the upper, and lower lip, lateral and ventral surface of tongue, hard palate and retro molar regions. The case was managed with corticosteroids.</p>","PeriodicalId":72274,"journal":{"name":"Archive of clinical cases","volume":"9 4","pages":"157-160"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/9d/83/acc-09-04-157.PMC9769071.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10574061","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Adult onset Xanthogranuloma presenting as a solitary laryngeal localization: case report and review of literature. 成人发性黄色肉芽肿表现为喉部单发定位:病例报告及文献回顾。
Archive of clinical cases Pub Date : 2022-01-01 DOI: 10.22551/2022.37.0904.10221
Gianluca Velletrani, Beatrice Francavilla, Valentina Rosati, Belen Padial, Lucia Anemona, Stefano Di Girolamo
{"title":"Adult onset Xanthogranuloma presenting as a solitary laryngeal localization: case report and review of literature.","authors":"Gianluca Velletrani,&nbsp;Beatrice Francavilla,&nbsp;Valentina Rosati,&nbsp;Belen Padial,&nbsp;Lucia Anemona,&nbsp;Stefano Di Girolamo","doi":"10.22551/2022.37.0904.10221","DOIUrl":"https://doi.org/10.22551/2022.37.0904.10221","url":null,"abstract":"<p><p>Juvenile Xanthogranuloma (XG) is a rare disorder that belongs to the heterogeneous group of histiocytic neoplasms, characterized by a clonal expansion of non-Langerhans cell histiocytes that share a dermal macrophage phenotype. Although the head and neck region is the most common reported site of involvement by the Juvenile Xanthogranuloma family, laryngeal localization is extremely rare. We report a unique case of Adult Onset Xanthogranuloma with subglottic localization, presenting as a solitary laryngeal mass without other systemic or cutaneous lesions. A review of the previously described cases of laryngeal Xanthogranuloma has been performed, highlighting 7 cases of Juvenile Xanthogranuloma and only 3 cases of Adult Onset Xanthogranuloma. Despite the extreme rarity of laryngeal localization of XG, this histiocytic neoplasm should be considered as a differential diagnosis for laryngeal masses causing airway obstruction, even in the absence of other concomitant manifestations.</p>","PeriodicalId":72274,"journal":{"name":"Archive of clinical cases","volume":"9 4","pages":"145-149"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/de/b7/acc-09-04-145.PMC9769079.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10511187","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Gut-brain axis: Review on the association between Parkinson's disease and plant lectins. 肠脑轴:帕金森病与植物凝集素关系的研究进展。
Archive of clinical cases Pub Date : 2022-01-01 DOI: 10.22551/2022.37.0904.10228
Kayvon Moin, Carly Funk, Meagan Josephs, Kyle Coombes, Madeleine Yeakle, Dhir Gala, Mohammad Ahmed-Khan
{"title":"Gut-brain axis: Review on the association between Parkinson's disease and plant lectins.","authors":"Kayvon Moin,&nbsp;Carly Funk,&nbsp;Meagan Josephs,&nbsp;Kyle Coombes,&nbsp;Madeleine Yeakle,&nbsp;Dhir Gala,&nbsp;Mohammad Ahmed-Khan","doi":"10.22551/2022.37.0904.10228","DOIUrl":"https://doi.org/10.22551/2022.37.0904.10228","url":null,"abstract":"<p><p>Gastrointestinal (GI) involvement in the pathogenesis of Parkinson's Disease (PD) has been widely recognized and supported in recent literature. Prospective and retrospective studies found non-motor symptoms within the GI, specifically constipation, precede cardinal signs and cognitive decline by almost 20 years. In 2002, Braak et al. were the first to propose that PD is a six-stage propagating neuropathological process originating from the GI tract (GIT). Aggregated α-synuclein (α-syn) protein from the GIT is pathognomonic for the development of PD. This article reviews the current literature from the past 10 years as well as original research found in PubMed on the combined effects of enteric glial cells and lectins on the development of Parkinson's Disease. Studies have found that these aggregated and phosphorylated proteins gain access to the brain via retrograde transport through fast and slow fibers of intestinal neurons. Plant lectins, commonly found within plant-based diets, have been found to induce Leaky Gut Syndrome and can activate enteric glial cells, causing the release of pro-inflammatory cytokines. Oxidative stress on the enteric neurons, caused by a chronic neuro-inflammatory state, can cause a-syn aggregation and lead to Lewy Body formation, a hallmark finding in PD. Although the current literature provides a connection between the consumption of plant lectins and the pathophysiology of PD, further research is required to evaluate confounding variables such as food antigen mimicry and other harmful substances found in our diets.</p>","PeriodicalId":72274,"journal":{"name":"Archive of clinical cases","volume":"9 4","pages":"177-183"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/cc/90/acc-09-04-177.PMC9769076.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10511189","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Peripheral T-Cell Lymphoma, Not Otherwise Specified - a case report and short literature review. 外周t细胞淋巴瘤,无其他特异性- 1例报告和简短的文献回顾。
Archive of clinical cases Pub Date : 2022-01-01 DOI: 10.22551/2022.37.0904.10220
Rafael Henriques de Figueiredo, Beatriz Simão Parreira, Pedro Amoroso Canão, Leila Cardoso, Elsa Fonseca, Jorge Almeida
{"title":"Peripheral T-Cell Lymphoma, Not Otherwise Specified - a case report and short literature review.","authors":"Rafael Henriques de Figueiredo,&nbsp;Beatriz Simão Parreira,&nbsp;Pedro Amoroso Canão,&nbsp;Leila Cardoso,&nbsp;Elsa Fonseca,&nbsp;Jorge Almeida","doi":"10.22551/2022.37.0904.10220","DOIUrl":"https://doi.org/10.22551/2022.37.0904.10220","url":null,"abstract":"<p><p>Peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS) is the most common subgroup of peripheral T-cell lymphomas (PTCL), and constitutes a diagnosis of exclusion. At presentation, most patients exhibit B symptoms and generalized lymphadenopathy, with or without concomitant extra-nodal involvement. We present a case of a man admitted to the hospital with B symptoms, generalized lymphadenopathy and a pruritic exanthema. Laboratory workup reveled persistent eosinophilia and malignant hypercalcemia. The excisional lymph node biopsy diagnosed PTCL-NOS, and the skin biopsy demonstrated a lichenoid dermatitis, compatible with the presumptive clinical diagnosis of a drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome. The patient was treated with topical betamethasone with good overall response, and initiated the first cycle of chemotherapy before discharge. This case report describes a PTCL-NOS with a concomitant non-lymphoproliferative disease, the challenging diagnostic workup of the two diseases and reinforces the most important features of the lymphoproliferative neoplasm.</p>","PeriodicalId":72274,"journal":{"name":"Archive of clinical cases","volume":"9 4","pages":"140-144"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/8b/51/acc-09-04-140.PMC9769073.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10511191","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Botulinum toxin as an adjunct for severe Dupuytren's contracture treated with collagenase injections. 肉毒杆菌毒素辅助胶原酶注射治疗严重双膝挛缩。
Archive of clinical cases Pub Date : 2022-01-01 DOI: 10.22551/2022.37.0904.10218
Keith A Denkler, Justin Cheng, Siyou Song, Scott Hansen
{"title":"Botulinum toxin as an adjunct for severe Dupuytren's contracture treated with collagenase injections.","authors":"Keith A Denkler,&nbsp;Justin Cheng,&nbsp;Siyou Song,&nbsp;Scott Hansen","doi":"10.22551/2022.37.0904.10218","DOIUrl":"https://doi.org/10.22551/2022.37.0904.10218","url":null,"abstract":"<p><p>Even with Dupuytren's proximal interphalangeal joint (PIPJ) contractures successfully released, volar flexor muscle memory can contribute to persistent contracture. We report using botulinum toxin (BoNTA) to the flexor digitorum superficialis muscle (FDS) to reduce flexor tone during recovery. <b>Case Description</b>. Two Collagenase clostridium histolyticum (CCH) injections were given to a patient with a -90° (PIPJ) contracture and a -35° degree distal interphalangeal joint (DIPJ) contracture. At the first CCH injection, 20 μ total of the Botulinum toxin was placed into the FDS muscle. Manipulation occurred at one week. A second injection of CCH followed by manipulation one week later occurred at two months, but no additional BoNTA was given. The final follow-up measurements at 53 months showed a PIPJ of -30° and a DIPJ of 0°. Total active motion improved from 140° to 240°. Outcomes of any treatment for severe Dupuytren's PIPJ contractures of the little finger are unpredictable and are often considered for staged external expansion or even salvage procedures. BoNTA injections weaken flexor tone in tendon repairs and for treating hypertonic muscles after strokes. <b>Conclusion</b>. We hypothesized that BoNTA injection could enhance the outcomes of DC treatment by inhibiting volar flexion forces during the recovery phase. The following case illustrates that using a BoNTA injection may have helped treat a severe PIPJ contracture. BoNTA injections need further research and controlled clinical trials to discover their proper role in Dupuytren's contractures treated via CCH injections, fasciotomies, and fasciectomies.</p>","PeriodicalId":72274,"journal":{"name":"Archive of clinical cases","volume":"9 4","pages":"133-135"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/e5/5e/acc-09-04-133.PMC9769080.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10520982","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bilateral recurrent laryngeal nerve palsy following anterior cervical surgery subsequent to contralateral apical lung radiotherapy. 对侧肺根尖放疗后颈椎前路手术后双侧喉返神经麻痹。
Archive of clinical cases Pub Date : 2022-01-01 DOI: 10.22551/2022.37.0904.10223
Timothy Woodacre, Nooshin Jahromi, Geraldine Goh, Thomas Clifton, David Dillon
{"title":"Bilateral recurrent laryngeal nerve palsy following anterior cervical surgery subsequent to contralateral apical lung radiotherapy.","authors":"Timothy Woodacre,&nbsp;Nooshin Jahromi,&nbsp;Geraldine Goh,&nbsp;Thomas Clifton,&nbsp;David Dillon","doi":"10.22551/2022.37.0904.10223","DOIUrl":"https://doi.org/10.22551/2022.37.0904.10223","url":null,"abstract":"<p><p>Unilateral recurrent laryngeal nerve palsy is a potential complication of the anterior approach for cervical surgery. It is a rare complication of radiotherapy to the neck. Only one case has been reported following radiotherapy apical lung cancer. It can result in unilateral vocal cord paralysis. We report a patient who demonstrated bilateral vocal cord paralysis immediately following right-sided anterior cervical surgery, with significant consequences, including aphonia, respiratory distress and subsequent takotsubo cardiomyopathy. She was diagnosed with acute, (temporary) post-operative right recurrent laryngeal nerve palsy, on the background of undetected and previously asymptomatic left recurrent laryngeal nerve palsy following radiotherapy for left apical lung cancer. The possibility of recurrent laryngeal nerve palsy should be considered in patients with previous apical lung cancer and/ or radiotherapy. Patents undergoing subsequent anterior cervical surgery should be considered for the appropriate precautions in the form of same-side surgery or pre-operative investigation for vocal cord paralysis.</p>","PeriodicalId":72274,"journal":{"name":"Archive of clinical cases","volume":"9 4","pages":"154-156"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/cc/96/acc-09-04-154.PMC9769081.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10511188","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A rare presentation of pulmonary thromboembolism as seizure. 罕见的肺血栓栓塞表现为癫痫发作。
Archive of clinical cases Pub Date : 2022-01-01 DOI: 10.22551/2022.37.0904.10219
Toktam Alirezaei, SeyedehFatemeh Mousavi, Hamed Hesami
{"title":"A rare presentation of pulmonary thromboembolism as seizure.","authors":"Toktam Alirezaei,&nbsp;SeyedehFatemeh Mousavi,&nbsp;Hamed Hesami","doi":"10.22551/2022.37.0904.10219","DOIUrl":"https://doi.org/10.22551/2022.37.0904.10219","url":null,"abstract":"<p><p>Acute pulmonary thromboembolism is a critical and sometimes fatal event that is difficult for clinicians to diagnose because of its various initial manifestations. Here, we report a previously healthy 50-year-old man without any history of seizures who presented to the emergency ward with the new-onset seizure. Neurology consult was performed, but found no focal neurological deficits. The diagnosis of massive pulmonary embolism was confirmed by echocardiography and pulmonary CT angiography. Alteplase and heparin with therapeutic dosage were started for the patient. After initiating treatment, patient's dyspnea, arterial O2 saturation, and general condition were significantly improved. Echocardiography was repeated and showed a smaller right ventricle size and lower pulmonary artery pressure than the first echocardiography.</p>","PeriodicalId":72274,"journal":{"name":"Archive of clinical cases","volume":"9 4","pages":"136-139"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/29/86/acc-09-04-136.PMC9769075.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10511192","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Triple whammy: a rare case of epithelioid hemangioendothelioma with synchronous angiomyomatous hamartoma complicated by Actinomyces meyeri. 三重打击:一例罕见的上皮样血管内皮瘤合并同步血管肌瘤错构瘤并发放线菌。
Archive of clinical cases Pub Date : 2021-12-29 eCollection Date: 2021-01-01 DOI: 10.22551/2021.32.0803.10187
Nariman Khan, Saadia Waheed, Rahaf Alkhateb
{"title":"Triple whammy: a rare case of epithelioid hemangioendothelioma with synchronous angiomyomatous hamartoma complicated by <i>Actinomyces meyeri</i>.","authors":"Nariman Khan,&nbsp;Saadia Waheed,&nbsp;Rahaf Alkhateb","doi":"10.22551/2021.32.0803.10187","DOIUrl":"https://doi.org/10.22551/2021.32.0803.10187","url":null,"abstract":"<p><p>Epithelioid hemangioendothelioma is a rare vascular malignancy that originates from vascular endothelial or pre-endothelial cells and is composed of epithelioid or histiocytoid cells. This malignancy has an incidence of approximately one per one million individuals and can occur in various regions of the body including the lungs, liver, bones, and soft tissues. The behavior of this cancer can range from indolent to aggressive and diagnosis and treatment are often delayed due to variable presentations and lack of established treatment guidelines. Here we present the case of a 27-year-old Hispanic male that presented with right groin pain, abdominal pain, and a fifty-pound weight loss over one year. The patient had a complex hospital course during which he was found to have an angiomyomatous hamartoma of his right groin area, postsurgical right inguinal wound infection with <i>Actinomyces meyeri</i>, and epithelioid hemangioendothelioma distal to the right iliac bifurcation. The patient is currently pending further imaging studies to evaluate candidacy for surgical resection and following with oncology for chemotherapeutic options.</p>","PeriodicalId":72274,"journal":{"name":"Archive of clinical cases","volume":"8 3","pages":"56-61"},"PeriodicalIF":0.0,"publicationDate":"2021-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/46/9a/acc-08-03-56.PMC8717002.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39662314","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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