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1.
BMJ Case Rep ; 14(7)2021 Jul 27.
Artigo em Inglês | MEDLINE | ID: mdl-34315734

RESUMO

A 66-year-old Asian woman presented with severe kidney injury, microscopic haematuria and subnephrotic range proteinuria with elevated serum anti-glomerular basement membrane (anti-GBM) titre. She had a history of renal cell carcinoma. Renal biopsy revealed dual pathology with immunofluorescence showing 3+ linear glomerular IgG staining and 3+ IgA mesangial staining. Cellular crescents were present on light microscopy and electron microscopy revealed increased mesangial matrix. She was treated with plasma exchange and immunosuppression and remained in stage 4 chronic kidney disease. This case describes the coexistence of anti-GBM disease and IgA nephropathy, a phenomenon not well described in the literature. The report also explores the association of malignancy and glomerulonephritis as well as the role of genetics and the utility of human leukocyte antigen (HLA) typing in risk stratification.


Assuntos
Doença Antimembrana Basal Glomerular , Carcinoma de Células Renais , Glomerulonefrite por IGA , Neoplasias Renais , Idoso , Doença Antimembrana Basal Glomerular/complicações , Doença Antimembrana Basal Glomerular/diagnóstico , Autoanticorpos , Carcinoma de Células Renais/complicações , Feminino , Membrana Basal Glomerular , Glomerulonefrite por IGA/complicações , Glomerulonefrite por IGA/diagnóstico , Humanos , Neoplasias Renais/complicações
4.
Am J Surg Pathol ; 41(10): 1433-1442, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-28731868

RESUMO

Inflammatory myofibroblastic tumor (IMT) of the female genital tract is under-recognized. We investigated the prevalence of ALK-positive IMT in lesions previously diagnosed as gynecologic smooth muscle tumors. Immunohistochemistry (IHC) for ALK was performed on tissue microarrays of unselected tumors resected from 2009 to 2013. Three of 1176 (0.26%) "leiomyomas" and 1 of 44 (2.3%) "leiomyosarcomas" were ALK IHC positive, confirmed translocated by fluorescence in situ hybridization (FISH) and therefore more appropriately classified as IMT. On review significant areas of all 4 tumors closely mimicked smooth muscle tumors morphologically, but all showed at least subtle/focal features suggesting IMT. Recognizing that the distinction between IMT and leiomyoma/leiomyosarcoma can be subtle, we then reviewed 1 hematoxylin and eosin slide from each patient undergoing surgery for "leiomyoma" from 2014 to 2017 and selected cases for ALK IHC with a low threshold. Of these, 30 of 571 (5.3%) underwent IHC. Two were confirmed to be IHC positive and FISH rearranged. Of the 6 IMTs, only 1 tumor with a previous diagnosis of leiomyosarcoma, an infiltrative margin and equivocal necrosis, metastasized. Of note it demonstrated a less aggressive clinical course compared with most metastatic leiomyosarcomas (alive with disease at 6 y). The patient was subsequently offered crizotinib to which she responded rapidly. In conclusion, IMTs may closely mimic gynecologic smooth muscle tumors. IMTs account for at least 5 of 1747 (0.3%) tumors previously diagnosed as leiomyoma and 1 of 44 (2.3%) as leiomyosarcoma. These tumors may be recognized prospectively with awareness of subtle/focal histologic clues, coupled with a low threshold for ALK IHC.


Assuntos
Doenças dos Genitais Femininos/patologia , Granuloma de Células Plasmáticas/patologia , Receptores Proteína Tirosina Quinases/análise , Adulto , Idoso , Idoso de 80 Anos ou mais , Quinase do Linfoma Anaplásico , Feminino , Doenças dos Genitais Femininos/metabolismo , Granuloma de Células Plasmáticas/metabolismo , Humanos , Imuno-Histoquímica , Pessoa de Meia-Idade , Receptores Proteína Tirosina Quinases/metabolismo , Adulto Jovem
5.
Am J Surg Pathol ; 41(1): 75-81, 2017 01.
Artigo em Inglês | MEDLINE | ID: mdl-27635947

RESUMO

A quarter of patients with medullary thyroid carcinoma (MTC) have germline mutations in the RET proto-oncogene indicating MEN2. Therefore genetic testing is recommended for all patients presenting with MTC. Approximately 40% of MTCs have somatic RET mutations. Somatic mutations in the RAS genes are the next most common driver mutations and appear to be mutually exclusive with germline RET mutation. The single most common somatic RAS mutation is HRASQ61R (c.182A>G), reported in 4.6% to 11% of all MTCs. Mutation-specific immunohistochemistry (IHC) initially developed to identify the NRASQ61R mutation in melanoma (clone SP174) has proven highly sensitive and specific. Because the amino acid sequences for the HRAS and NRAS proteins at codon 61 are identical, we postulated that SP174 IHC would also identify the somatic HRASQ61R mutation. IHC with SP174 was performed on a tissue microarray of 68 patients with MTC including 13 (22.8%) with molecularly confirmed MEN2. Seven (10.3%) MTCs demonstrated positive staining. Six of these patients had already undergone germline RET mutation testing as part of clinical care and were all confirmed to be wild type, excluding the diagnosis of MEN2. All SP174 immunohistochemically positive MTCs were proven to have HRASQ61R mutation (and lack KRASQ61R and NRASQ61R) by Sanger sequencing. All MEN2 patients showed negative staining. We conclude that IHC with SP174 is highly specific for the HRASQ61R mutation in MTC. Because current data suggest that this mutation is mutually exclusive with germline RET mutation, IHC may also have a role in triaging formal genetic testing for MEN2.


Assuntos
Biomarcadores Tumorais/genética , Carcinoma Neuroendócrino/genética , Análise Mutacional de DNA/métodos , Neoplasia Endócrina Múltipla/diagnóstico , Proteínas Proto-Oncogênicas p21(ras)/genética , Neoplasias da Glândula Tireoide/genética , Adulto , Idoso , Idoso de 80 Anos ou mais , Anticorpos Monoclonais , Biomarcadores Tumorais/análise , Carcinoma Neuroendócrino/diagnóstico , Feminino , GTP Fosfo-Hidrolases/genética , Testes Genéticos , Humanos , Imuno-Histoquímica/métodos , Masculino , Proteínas de Membrana/genética , Pessoa de Meia-Idade , Neoplasia Endócrina Múltipla/genética , Reação em Cadeia da Polimerase , Proto-Oncogene Mas , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz , Neoplasias da Glândula Tireoide/diagnóstico , Análise Serial de Tecidos , Adulto Jovem
6.
J Med Case Rep ; 10: 64, 2016 Mar 18.
Artigo em Inglês | MEDLINE | ID: mdl-26987706

RESUMO

BACKGROUND: Distinguishing an atypical lipomatous tumor/well-differentiated liposarcoma from a benign lipomatous tumor on morphology alone can be difficult and there is an established role for MDM2 fluorescent in situ hybridization studies in making this differential diagnosis. There is no literature on the role for MDM2 fluorescent in situ hybridization studies in distinguishing between a well-differentiated liposarcoma with extreme fibrosis and a fibrosing inflammatory pseudotumor. CASE PRESENTATION: We report the case of a 76-year-old Australian woman initially diagnosed by an excision biopsy with a retroperitoneal fibrosing inflammatory pseudotumor. She was then diagnosed 5 years later with a pleomorphic undifferentiated sarcoma. Upon review of the original resection specimen, we were able to show that the tumor demonstrated MDM2 amplification. MDM2 amplification was also present in some adjacent bland adipose tissue, and also in the tumor recurrence as a pleomorphic undifferentiated sarcoma. CONCLUSION: Taken together, our findings provide strong evidence that the original tumor was a misdiagnosed well-differentiated liposarcoma with extreme fibrosis, and the pleomorphic undifferentiated sarcoma represented a recurrence of the same tumor with dedifferentiation.


Assuntos
Granuloma de Células Plasmáticas/diagnóstico , Inflamação/patologia , Lipossarcoma/diagnóstico , Fibrose Retroperitoneal/diagnóstico , Neoplasias de Tecidos Moles/diagnóstico , Idoso , Biomarcadores Tumorais , Diagnóstico Diferencial , Feminino , Amplificação de Genes , Granuloma de Células Plasmáticas/genética , Humanos , Hibridização in Situ Fluorescente , Recidiva Local de Neoplasia , Proteínas Proto-Oncogênicas c-mdm2/genética , Fibrose Retroperitoneal/genética , Fibrose Retroperitoneal/imunologia , Neoplasias de Tecidos Moles/genética , Neoplasias de Tecidos Moles/imunologia
7.
ANZ J Surg ; 84(6): 424-8, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24405988

RESUMO

BACKGROUND: Traumatic brain injury (TBI) is common and is a leading cause of presentations to emergency departments. Understanding the epidemiology of TBI can aid in improving overall management and identifying opportunities for prevention. Currently, there is a paucity of data on paediatric TBI in NSW. The purpose of this study was to determine the demographics, causes, treatment and outcome of TBI at The Children's Hospital at Westmead (CHW), a large trauma referral paediatric hospital. METHODS: A retrospective chart review was conducted of patients admitted to CHW emergency from 2006 to 2011 with a TBI. Patients who presented to the emergency department and had a history of TBI with either symptoms of concussion and/or positive computed tomography (CT) findings of head injury were selected. Information regarding demographics, injury pattern, CT findings, treatment and outcome were retrieved. RESULTS: Over the 6-year period, there were 1489 presentations at the CHW. Of these, 65% were male and 35% were female. The mean age was 7 years. A total of 93% were classified as mild, 1.5% as moderate and 5.5% as severe. Sports and recreational injuries accounted for 26% of all TBI presentations, while motor vehicle accidents (MVAs) accounted for 77% of all TBI deaths. Sixty-two per cent of children underwent a CT brain, and of those, 40% were normal. CONCLUSION: The majority of TBI are mild in nature, with younger children and males at greatest risk. There was a low rate of operative intervention and a high rate of good outcomes. Many injuries may be preventable with the adaptation of better public health education programmes, particularly in very young children and those related to MVAs.


Assuntos
Lesões Encefálicas/diagnóstico por imagem , Lesões Encefálicas/epidemiologia , Centros de Traumatologia , Adolescente , Distribuição por Idade , Lesões Encefálicas/terapia , Criança , Pré-Escolar , Estudos de Coortes , Terapia Combinada , Intervalos de Confiança , Feminino , Escala de Coma de Glasgow , Hospitais Pediátricos , Humanos , Lactente , Recém-Nascido , Escala de Gravidade do Ferimento , Masculino , New South Wales/epidemiologia , Prognóstico , Estudos Retrospectivos , Distribuição por Sexo , Taxa de Sobrevida , Tomografia Computadorizada por Raios X/métodos
8.
J Emerg Nurs ; 39(5): e79-81, 2013 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-23657008

RESUMO

Immobilization of fractures with plaster of Paris is a mainstay of management of stable, nondisplaced fractures not requiring fixation. However, application techniques can be variable and are often ineffective after the patient is discharged because of weakness and wear of the plaster. This can lead to displacement of fractures and inadequate analgesia. We describe a simple, inexpensive, effective technique to ensure plaster strength and immobilization.


Assuntos
Sulfato de Cálcio , Moldes Cirúrgicos , Fraturas Ósseas/terapia , Contenções , Medicina de Emergência/instrumentação , Medicina de Emergência/métodos , Humanos , Imobilização/instrumentação , Imobilização/métodos , Ossos Metacarpais/lesões , Procedimentos Ortopédicos/instrumentação , Procedimentos Ortopédicos/métodos , Rádio (Anatomia)/lesões , Polegar
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