Ortíz Hidalgo, Carlos Federico
Main Affiliation
Preferred name
Ortíz Hidalgo, Carlos Federico
Official Name
Ortíz Hidalgo, Carlos Federico
ORCID
0000-0002-2456-7402
Researcher ID
DWN-7833-2022
Scopus Author ID
7003618204
73 results
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Item type:Publication, Mujer de 33 años de edad con leve dolor toracoabdominal derecho de seis años de evolución, súbitamente agudizado(2011) ;Cárdenas-Escudero, Mara A. ;Shuchleib-Chaba, Samuel ;Muruchi-Garrón, Germán Walter ;León-Bojorge, Beatriz deWe present a case of a benign hybrid nerve sheath tumor showing features of both cellular schwannoma and perineurioma. The patient was a 33 year-old female who presented with a 6 month history of pain in the thorax-lumbar region. Axial CT and MIR images showed and homogeneously enhancing solid oval mass involving the left paravertebra region in contact with the vertebral foramina T9-T11. Morphologically the tumor presented a well formed capsule and showed a uniform highly spindle cell proliferation. The spindle cells were arranged in whorls and intersecting fascicles with focal intervening sclerosis and relatively uniform cellularity with a prominent perivascular lymphocytic infiltrate. No cytological atypia, necrosis or mitoses were present. A second cell component was present composed of spindle-shaped cells with inconspicuous bipolar, pale, eosinophilic cytoplasm with oval nuclei. By immunohistochemistry there was a diffuse staining for S-100, and the elongated bipolar cells were EMA, Glut-1 and Claudin-1. To our knowledge this is the first reported case of a hybrid cellular schwannoma/perineurioma. ©Gaceta Médica de México2 9 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, History of Leukemia, RevisitedPurpose of the Review: Provide a general historical overview of leukemia, emphasizing the early discoveries that led to its characterization. Recent Findings: Leukemia recognition began in the late 19th century with the advent of the microscope. Leeuwenhoek and Swammerdam described erythrocytes, while Lieutaud first observed globuli albicantes, later identified as lymphocytes by Hewson. Early case studies by Velpeau, Donné, Bennett, Craigie, Virchow, and Fuller suggested that leukocytosis could occur without infection. Virchow coined the term “leukemia,” while Bennett proposed “leucocythemia.” Neumann identified the bone marrow as the source of blood cells and leukemia, coining the term “myelogenous leukemia,” and Ehrlich classified leukemia into myeloid and lymphoid types. In 1914, Boveri linked chromosomal abnormalities to cancer, and in 1960, Nowell and Hungerford discovered the Philadelphia chromosome. The use of mustard gas in WWI led to the development of chemotherapy drugs like chlorambucil and busulfan. The Human Genome Project further advanced leukemia diagnosis and treatment. Summary: Leukemia, like many diseases, has evolved due to changes in causative factors such as viruses, bacteria, and genetic mutations, which have impacted its pathogenesis and treatment. It will undoubtedly continue to evolve, with new scientists working towards a cure for this devastating disease. ©The author ©Current Oncology Reports ©Springer Science and Business Media LLC.28 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, El profesor y la costurera: Un episodio de la vida de Jacob HenleJacob Henle was a great German anatomist and one of the most important histologists of all times. One of the most commonly used eponymous terms in renal histology is the loop of Henle, but many other anatomical and pathological findings are associated with his name. During his stay in Zurich he fell in love with Elise Egolff who worked as a maid and seamstress in the house of one of his friends. No one could ever imagine how the wide social chasm that separated the servant-girl and the professor could be bridged. Henle arranged for his sister Marie to educate Elise and give her social polish. In a short time Elise was transformed into a lady of the world. A year and a half later Jacob and Elise were married. This episode inspired the novelist Auerbach to write the novel “The Professor’s Wife”, and the play “Pygmalion” by George B Shaw. (Gac Med Mex. 2015;151:819-27). © Gaceta Médica de México.2 9 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Small-Cell Plasmacytoma With Prominent Myxoid Stroma Mimicking a Soft-Tissue Neoplasm(2009) ;Lara-Torres, César Octavio ;Gómez-Plata, EduardoIn the majority of cases, histological diagnosis of plasma cell tumor can be made without difficulty; however, a proportion of them can represent a diagnostic challenge due to the wide spectrum of phenotypes that neoplastic plasma cells may exhibit. Numerous cytological and architectural variants have been well documented. Cytological, plasma cell tumors may show small, cleaved, multilobated, monocytoid, pleomorphic, histiocytoid, oncocytic, or clear cells. © International Journal of Surgical Pathology2Scopus© Citations 2 12 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Sarcoma histiocítico. Criterios diagnósticos histopatológicos e inmunohistoquímicos y sus diagnósticos diferenciales(2011) ;García-Gutiérrez, MónicaHistiocytic sarcoma (HS) is a rare malignant tumor, originating from bone marrow-derived myeloid stem cells, showing morphologic and immunophenotipic evidence of mature tissue histiocytes (macrophages). HS arises in lymph nodes and extranodal sites such as skin, soft tissues and particularly the gastrointestinal tract, often presenting with clinically advanced disease and pursuing and aggressive clinical course. The diagnosis of HS relies predominantly on the immunohistochemical features of the histiocytic lineage, and the exclusion of large cell lymphoma and other poorly differentiated large cell malignancies such as, carcinomas and melanomas.© Gaceta Mexicana de Oncología1 8 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Linfoma anaplásico de células grandes : estudio clínico-patológico e inmunohistoquímica de 20 casos clasificados de acuerdo a la revisión de la Organización Mundial de la Salud de neoplasias linfoides de 2016(2022) ;Sevilla Lizcano, Diana BrisaAnaplastic large cell lymphoma (ALCL) is a type of non-Hodgkin lymphoma composed of CD30-positive neoplastic cells. The 2016 revision of the WHO classification of lymphoid neoplasms includes anaplastic lymphoma kinase (ALK) positive, ALK negative and breast implant associated ALCL. ALCL have distinct clinical and prognostic features between positive and negative cases. ALK-1 positive cases mostly occur in the first three decades of life while patients with ALK-1 negative are older. ALCL exhibit a very broad range of cytology appearances that include common pattern, lymphohistiocytic pattern, small-cell pattern, Hodgkin-like pattern and composite pattern. By definition, ALCL show strong CD30 staining on the cell membrane and in the Golgi region and the majority are epithelial membrane antigen positive, express one or more T-cell or Natural Killer antigens and are constantly negative for Epstein-Barr virus. We present the clinicopathologic and immunohistochemical analysis of 20 cases of ALCL studied at a single institution, classified according to the 2016 revision of lymphoid neoplasms. Nine cases were ALK-1 positive, ten ALK-1 negative, and one case as a breast implant associated ALCL ALK-1 negative. © 2017 Sociedad Mexicana de Oncología.2 10Scopus© Citations 1 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Enfermedad de Castleman. Análisis histopatológico e inmunohistoquímico de treinta y nueve casos(2017) ;Brisa Sevilla-Lizcano, Diana ;Frias-Soria, Christian LizetteIntroduction: Castleman disease (CD) is a rare lymphoproliferative that comprises two distinct clinical subtypes (unicentric and multicentric) and has two basic histopathology patterns that are hyaline-vascular (HV) and plasma-cell (PC) type. Some cases of multicentric PC disease are associated with HHV-8 infection. Objective: To present the histopathologic and immunohistochemical characteristics of 39 cases of CD. Methods: A review of cases with the diagnosis CD from the files of the Department of Pathology of the ABC Medical Centre in Mexico City was performed. Thirty-nine cases of CD were identified, and a detailed paraffin immunophenotypic study of 9 of them was completed using desmin, cytokeratin OSCAR (CO) and Epidermal growth factor receptor (EGFR), to evaluate the dendritic cell population. ©Gaceta Médica de México.Scopus© Citations 7 2 10 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Well-differentiated (Marschalko-type) plasmacytoma resembling thyroid follicular structures(2008) ;Lara-Torres, César OctavioDear Editor: Plasma cell neoplasms may display diverse cytoarchitectural variations, including a diffuse, nested, paragangliomatous, and angiomatoid arrangements [1]. We present herein a case of a well-differentiated (Marschalko-type) plasmacytoma in which neoplastic plasma cells arranged in a pseudofollicular configuration resemble thyroid follicles filled with ‘colloid-like’ material. © Journal of Hematopathology1 3Scopus© Citations 3 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Immunohistochemistry in Historical Perspective: Knowing the Past to Understand the PresentImmunohistochemistry is an extraordinary and extensively used technique whereby antibodies are used to detect antigens in cells within a tissue section. It has numerous applications in medicine, particularly in cancer diagnosis. It was Albert Hewett Coons, Hugh J Creech, Norman Jones, and Ernst Berliner who conceptualized and first implemented the procedure of immunofluorescence in 1941. They used fluorescein isothiocyanate (FITC)-labelled antibodies to localize pneumococcal antigens in infected tissues. Since then, with improvement and development of protein conjugation, enzyme labels have been introduced, such as peroxidase and alkaline phosphatase. The history of immunohistochemistry (IHC) combines physiology, immunology, biochemistry, and the work of various Nobel Prize laureates. From von Behring who was awarded de first Nobel Prize in 1901 for his work on serum therapy to the 1984 Nobel Prize for the discovery of monoclonal antibodies by Milstein, Kohler, and Jerne, IHC is a story of cooperation and collaboration which led to the development of this magnificent technique that is used daily in anatomical pathology laboratories worldwide. © Springer Nature.1 18Scopus© Citations 30 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Tumor rabdoide/teratoide atípico. Presentación de tres casos y revisión de la literatura(2001) ;Cuesta Mejías, Teresa Cristina ;León Bojorge, Beatriz de ;Rivas Hernández, Angélica ;Martínez Madrigal, FernandoCuevas, FranciscoIntroducción: El tumor rabdoide/teratoide atípico (TR/TA) del sistema nervioso central (SNC) ha emergido de una variante de meduloblastoma a una entidad clinicopatológica distintiva, durante la última década. Esto tiene importancia más que nosológica, ya que la supervivencia de cinco años prevista en los meduloblastomas es considerablemente mejor que la de 11 meses (promedio) mostrada por los TR/TA. Objetivo: Describir las principales características clinicopatológicas de una entidad recientemente reconocida, haciendo énfasis en su polimorfismo y diagnóstico diferencial. Pacientes y métodos: Se presenta el aspecto clínico, radiológico, citohistopatológico e inmunohistoquímico de tres TR/TA diagnosticados en el Hospital A.B.C. de la Ciudad de México. ©Revista de Neurología1 9Scopus© Citations 4
