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Your search keyword '"Lymphatic Diseases genetics"' showing total 7 results
Start Over Descriptor "Lymphatic Diseases genetics" Language spanish; castilian
7 results on '"Lymphatic Diseases genetics"'

2. [Familial hemophagocytic lymphohistiocytosis. Presentation of 2 cases in one family].

Author

Gamboa-Marrufo JD, Dorantes-Mesa S, Toledo-Cortina G, Rivera-Hernández F, Mejía-Domínguez A, Bello-González A, and Valencia-Mayoral P

Subjects
Bone Marrow pathology, Child, Preschool, Female, Humans, Infant, Liver pathology, Lymph Nodes pathology, Lymphatic Diseases pathology, Lymphocytosis pathology, Phagocytosis, Lymphatic Diseases genetics, Lymphocytosis genetics
Published
1986

3. [Familial erythrophagocytic lymphohistiocytosis with neonatal presentation].

Author

Arregui Sierra A, Arbelo López de Letona A, Quero Jiménez J, Pérez Rodríguez J, Alba Losada J, and Acebedo Barberá A

Subjects
Autophagy, Bone Marrow pathology, Erythrocytes, Female, Hemorrhage etiology, Hepatomegaly etiology, Humans, Infant, Newborn, Jaundice, Neonatal etiology, Lymph Nodes pathology, Lymphatic Diseases congenital, Lymphatic Diseases pathology, Splenomegaly etiology, Lymphatic Diseases genetics
Abstract

A neonatal case of familial erythrophagocytic lymphohistiocytosis is presented. Evolution was rapidly fatal under a course in which fever, hepatosplenomegaly, pancytopenia, severe coagulation alteration and jaundice were especially significant. Pathology findings after nine days of life, were all conclusive. Diagnostic difficulties of this uncommon entity in its' congenital form only once previously reported, are emphasized.

Published
1982

6. [Familial erythrophagocytic lymphohistiocytosis (author's transl)].

Author

Pineda G, Camacho Conde P, Alvarez Silván A, Navarro González J, González del Castillo J, and Sosa Alamo R

Subjects
Bone Marrow pathology, Child, Preschool, Humans, Liver pathology, Lymph Nodes pathology, Lymphatic Diseases pathology, Male, Phagocytes pathology, Lymphatic Diseases genetics
Abstract

A four-year old boy with familial erythrophagocytic lymphohistiocytosis is reported. The clinical picture was that of prolonged fever, hepato and splenomegaly, adenopathies and, in the terminal state, bleeding tendency and sligth jaundice. The laboratory data showed anemia, leucopenia and abnormal coagulation studies compatibles with disseminated intravascular clotting. The differential diagnosis with malignant histiocytosis is attempted from a histological point of view.

Published
1977

7. [Deteriorating natural killer activity in familial erythrophagocytic lymphohistiocytosis].

Author

Caballero García M, Mar Molinero F, Melián Machín A, Sánchez Díaz JI, Mollejo Villanueva M, Sotelo MT, and Nogales Espert A

Subjects
Antibody Formation, Humans, Immunity, Cellular, Infant, Lymphatic Diseases genetics, Lymphatic Diseases immunology, Lymphatic Diseases pathology, Male, Killer Cells, Natural physiopathology, Lymphatic Diseases physiopathology
Abstract

We report the occurrence of familial erythrophagocytic lymphohistiocytosis disease in a child who had greater involvement of the brain than of visceral organs. The diagnosis was made during life, allowing us to carry out biological, histological and immunological studies. The natural Killer activity was abolished in this patient. The combination chemotherapy--including systemic administration of VP 16-213, steroids and intrathecal methotrexate--, failed to stem the rapid course of the disease.

Published
1988

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