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1.
Rev Invest Clin ; 65 Suppl 2: s5-27, 2013 Jun.
Artigo em Espanhol | MEDLINE | ID: mdl-24459777

RESUMO

Non-Hodgkin lymphoma comprises a heterogeneous group of haematological malignancies, classified according to their clinic, anatomic-pathological features and, lately, to their molecular biomarkers. Despite the therapeutic advances, nearly half of the patients will die because of this disease. The new diagnostic tools have been the cornerstone to design recent therapy targets, which must be included in the current treatment guidelines of this sort of neoplasms by means of clinical trials and evidence-based medicine. In the face of poor diagnoses devices in most of the Mexican hospitals, we recommend the present diagnose stratification, and treatment guidelines for non-Hodgkin lymphoma, based on evidence. They include the latest and most innovative therapeutic approaches, as well as specific recommendations for hospitals with limited framework and therapy resources.


Assuntos
Linfoma não Hodgkin/diagnóstico , Linfoma não Hodgkin/terapia , Humanos , México
2.
Rev Med Inst Mex Seguro Soc ; 49(2): 185-90, 2011.
Artigo em Espanhol | MEDLINE | ID: mdl-21703146

RESUMO

BACKGROUND: Pancreatic cystic lesions (PCL) are identified in 1 % of patients who undergo abdominal computed tomography scans, because it is difficult to discriminate clinically between benign and malignant PCL. The PCL must be distinguished from inflammatory pseudocysts, which can have a similar radiographic appearance. The aim of this study was to review the incidence of PCL during 10 years. METHODS: Nineteen consecutive patients who underwent surgical resection of a cystic lesion of the pancreas during a 10-year period were reviewed. RESULTS: From 1998, 434 patients underwent to pancreatic surgery, 103 (25.75%) resulted with neoplasm of the pancreas and a PCL was diagnosed in 19 of them (18.44%). They were more common in women (n=15, 79%). The pathologic diagnosis was mucinous cystadenoma (n=6, 31.5%) followed by serous cystadenoma and solid cystic papilar tumor (n=4, 21%). Mucinous cystadenocarcinoma was diagnosed in a 77 year-old man and a serous cystadenocarcinoma was diagnosed in a 53 years-old woman; cystic degeneration of two insulinomas were diagnosed in a 71 year-old woman and a 32 year-old man (5.26%). CONCLUSIONS: PCLs represent a spectrum of associated diseases. The incidence of serous cystadenoma is lower in our experience.


Assuntos
Cisto Pancreático/epidemiologia , Neoplasias Pancreáticas/epidemiologia , Adulto , Idoso , Feminino , Humanos , Incidência , Masculino , Pessoa de Meia-Idade , Fatores de Tempo , Adulto Jovem
3.
Rev Gastroenterol Mex ; 69(4): 236-9, 2004.
Artigo em Espanhol | MEDLINE | ID: mdl-15765976

RESUMO

OBJECTIVE: The objective of this report is to describe the existence of a rare tumor that must be taken into consideration when studying the diagnosis of pancreatic tumors. CASE REPORT: A 20-year-old female with abdominal pain as an only manifestation was seen. The diagnosis of a pancreatic head and body tumor was made. During surgery, we found a tumor in the head and body of the pancreas that measured approximately 10 x 7 cm; histopathologic study revealed a solid and cystic papillary epithelial neoplasm of the pancreas. DISCUSSION: Frantz-Gruber tumor is a rare pancreatic tumor suspected during the evaluation of a young female with abdominal pain and confirmed during surgery. It is important to consider the existence of this tumor in the evaluation of patients with these characteristics; even if the tumor's biological behavior is benign Frantz-Gruber tumor is considered a low-grade malignant tumor


Assuntos
Adenocarcinoma Papilar/patologia , Carcinoma Papilar/patologia , Cistadenocarcinoma Papilar/patologia , Neoplasias Pancreáticas/patologia , Adulto , Feminino , Humanos , Neoplasias Pancreáticas/classificação , Neoplasias Pancreáticas/diagnóstico
4.
Cir Cir ; 71(2): 145-9, 2003.
Artigo em Espanhol | MEDLINE | ID: mdl-19764143

RESUMO

Rhinocerebral mucormycosis is a fulminant fungal disease that typically presents acutely in patients with diabetic ketoacidosis or immunosuppression. The case of a 55 year-old male patient is presented; the patient experienced chronic infection that involved nose, paranasal sinuses, hard palate, orbit, pterygopalatine fossa, infratemporal fossa with cavernous sinus thrombosis and compression of the internal carotid artery which develops in insidious manner after metabolic imbalance with predominantly ocular symptoms. The patient was managed with Amphotericin B and radical surgical debridement of affected tissue, the patient presenting cure without complications or added disabilities.


Assuntos
Encefalopatias/microbiologia , Infecções Fúngicas do Sistema Nervoso Central , Mucormicose , Doenças Nasais/microbiologia , Encefalopatias/diagnóstico , Encefalopatias/terapia , Infecções Fúngicas do Sistema Nervoso Central/diagnóstico , Infecções Fúngicas do Sistema Nervoso Central/terapia , Doença Crônica , Humanos , Masculino , Pessoa de Meia-Idade , Mucormicose/diagnóstico , Mucormicose/terapia , Doenças Nasais/diagnóstico , Doenças Nasais/terapia
5.
Rev Gastroenterol Mex ; 67(3): 199-201, 2002.
Artigo em Espanhol | MEDLINE | ID: mdl-12653059

RESUMO

BACKGROUND: Leukemic infiltration of perianal skin (leukemia cutis) is quite uncommon, and may consist of no diffuse infiltration, erythema, ulceration, fistula, and abscess. Diagnosis may be established by biopsy and adequate hematologic studies. Treatment must be conservative in patients with poorly controlled disease (sitz baths, antibiotics, radiotherapy), and surgical in patients with risk of fulminant sepsis and death. OBJECTIVE: To report a case of leukemic perianal infiltration with atypical ulcerated lesion. CASE REPORT: Female patient, 21 years of age with diagnosis of AML M7, began with perianal pain posterior to evacuation associated with bleeding; at perianal examination we found anterior atypical ulcerated lesion. We carried out a biopsy under suspicion of leukemic infiltration corroborated by histopathology. The patient received conservative treatment. CONCLUSIONS: We must suspect leukemic infiltration in patients with anal symptoms and effect close surveillance. Prognosis depends on control of hematologic disease.


Assuntos
Canal Anal/patologia , Leucemia Mieloide Aguda/patologia , Infiltração Leucêmica/terapia , Pele/patologia , Adulto , Feminino , Humanos , Leucemia Mieloide Aguda/terapia
7.
Med. interna Méx ; 16(4): 226-228, jul.-ago. 2000. ilus, CD-ROM
Artigo em Espanhol | LILACS | ID: lil-302985

RESUMO

En este reporte se comunica el caso de un paciente con una infrecuente manifestación de la enfermedad de Hodgkin. Era un varón con antecedentes de alcoholismo crónico que sufría pancitopenia, derrame pleural y gran esplenomegalia. Al principio se pensó en cirrosis hepática con hiperesplenismo; sin embargo, debido a que no hubo datos de afección hepática y la anemia persistía a pesar de las hemotransfusiones, se decidió la esplenectomía. El estudio histopatológico reveló enfermedad de Hodgkin de variedad celularidad mixta. Más adelante se realizó una biopsia de hueso en la que se encontraron células neoplásicas similares a las encontradas en el bazo. En la revisión de la literatura sólo se identificaron reportes aislados.


Assuntos
Humanos , Masculino , Adulto , Doença de Hodgkin , Neoplasias Esplênicas , Biópsia por Agulha , Medula Óssea/patologia
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