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1. Full Text Clinical and laboratory profile of persons living with human immunodeficiency virus/acquired immune deficiency syndrome and histoplasmosis from a Colombian hospital
by Caceres, Diego H and Tobón, Angela M and Cleveland, Angela Ahlquist and Scheel, Christina M and Berbesi, Dedsy Y and Ochoa, Jesús and Restrepo, Angela and Brandt, Mary E and Chiller, Tom and Gómez, Beatriz L
American Journal of Tropical Medicine and Hygiene, ISSN 0002-9637, 10/2016, Volume 95, Issue 4, pp. 918 - 924
Histoplasmosis is common among persons living with human immunodeficiency virus/acquired immune deficiency syndrome (PLWHA) in Latin America, but its diagnosis... 
DIAGNOSIS | AMERICA | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | RISK-FACTORS | TUBERCULOSIS | AIDS | BRAZIL | EPIDEMIOLOGY | TROPICAL MEDICINE | HIV-INFECTED PATIENTS | FUNGAL-INFECTIONS | MANIFESTATIONS | Headache - etiology | Tuberculosis - physiopathology | Humans | Tuberculosis - complications | Coinfection - blood | Lymphadenopathy - etiology | Male | Alanine Transaminase - blood | Dyspnea - etiology | Skin Ulcer - etiology | Coinfection - physiopathology | Coinfection - complications | Histoplasmosis - complications | Karnofsky Performance Status | Splenomegaly - etiology | Adult | Female | Acquired Immunodeficiency Syndrome - blood | Tuberculosis - blood | HIV Infections - blood | Colombia | Abdominal Pain - etiology | Thrombocytopenia - etiology | Histoplasmosis - physiopathology | Cough - etiology | Nausea - etiology | Aspartate Aminotransferases - blood | Weight Loss | HIV Infections - complications | Vomiting - etiology | Diarrhea - etiology | HIV Infections - physiopathology | Histoplasmosis - blood | Acquired Immunodeficiency Syndrome - complications | Leukopenia - etiology | Hepatomegaly - etiology
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2. Full Text Clinical presentation of childhood leukaemia: a systematic review and meta-analysis
by Clarke, Rachel T and Van den Bruel, Ann and Bankhead, Clare and Mitchell, Christopher D and Phillips, Bob and Thompson, Matthew J
Archives of Disease in Childhood, ISSN 0003-9888, 10/2016, Volume 101, Issue 10, pp. 894 - 901
ObjectiveLeukaemia is the most common cancer of childhood, accounting for a third of cases. In order to assist clinicians in its early detection, we... 
Oncology | Haematology | PRIMARY-CARE | ACUTE LYMPHOBLASTIC-LEUKEMIA | PEDIATRICS | MYELOMONOCYTIC LEUKEMIA | HEMATOLOGIC FEATURES | CANCER | CHRONIC MYELOID-LEUKEMIA | ACUTE PROMYELOCYTIC LEUKEMIA | UNSELECTED SERIES | CHILDREN | MANIFESTATIONS | Contusions - etiology | Recurrence | Musculoskeletal Diseases - etiology | Abdominal Pain - etiology | Early Detection of Cancer | Humans | Gastrointestinal Diseases - etiology | Child, Preschool | Infant | Infection - etiology | Exanthema - etiology | Skin Diseases - etiology | Leukemia - complications | Hemorrhage - etiology | Adolescent | Fever - etiology | Splenomegaly - etiology | Leukemia - diagnosis | Child | Infant, Newborn | Hepatomegaly - etiology | Leukemia in children | Research | Diagnosis
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3. Full Text Cirrhosis in an active duty soldier with concomitant isolated polycystic disease and H63D homozygosity
by Madigan, Cory G and Wang, James Y
Military Medicine, ISSN 0026-4075, 08/2016, Volume 181, Issue 8, pp. e965 - e967
We report the case of a 45-year-old male soldier who was evaluated for a rapidly expanding hepatic mass following cholecystectomy and was eventually found to... 
LIVER-DISEASE | MEDICINE, GENERAL & INTERNAL | HEMOCHROMATOSIS | Cysts - etiology | Thrombosis - complications | Humans | Middle Aged | Cholecystitis - etiology | Male | Tomography, X-Ray Computed | Hemochromatosis - complications | Liver Diseases - etiology | Portal Vein - abnormalities | Cholangitis - complications | Splenomegaly - etiology | Liver Diseases - complications | Hemochromatosis - genetics | Liver Cirrhosis - etiology | Liver Diseases - genetics | Abdominal Pain - etiology | Military Personnel | Liver Cirrhosis - complications | California | Gynecomastia - etiology | Cysts - complications | Cholangitis - etiology | Transferrin - analysis | Homozygote | Cholangitis - surgery | Thrombosis - etiology | Cysts - genetics | Fever - etiology | Jaundice - etiology
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4. Full Text Anticoagulant therapy for nodular regenerative hyperplasia in a HIV-infected patient
by Bihl, Florian and Janssens, Filip and Boehlen, Francoise and Rubbia-Brandt, Laura and Hadengue, Antoine and Spahr, Laurent
BMC Gastroenterology, ISSN 1471-230X, 01/2010, Volume 10, Issue 1, pp. 6 - 6
Background: Nodular regenerative hyperplasia (NRH) has been recently recognized as an emergent cause of liver disease in HIV-infected patients. NRH may cause... 
NONCIRRHOTIC PORTAL-HYPERTENSION | GASTROENTEROLOGY & HEPATOLOGY | CHRONIC LIVER-DISEASE | ACTIVE ANTIRETROVIRAL THERAPY | DRUGS | TRANSPLANTATION | Ascites - etiology | Liver - pathology | Abdominal Pain - etiology | Lymph Nodes - pathology | Humans | Esophageal and Gastric Varices - etiology | Heparin, Low-Molecular-Weight - therapeutic use | Remission Induction | Hypertension, Portal - drug therapy | Ascites - diagnosis | Hyperplasia - etiology | Hyperplasia - pathology | Splenomegaly - diagnosis | Hypertension, Portal - etiology | Biopsy | HIV Infections - complications | Splenomegaly - etiology | Adult | Female | Esophageal and Gastric Varices - diagnosis | Case studies | Care and treatment | Anticoagulants (Medicine) | Dosage and administration | HIV infection | Hyperplasia
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5. Full Text Liver Disease in Autosomal Recessive Polycystic Kidney Disease: Clinical Characteristics and Management in Relation to Renal Failure
by Luoto, Topi T and Pakarinen, Mikko P and Jahnukainen, Timo and Jalanko, Hannu
Journal of Pediatric Gastroenterology and Nutrition, ISSN 0277-2116, 08/2014, Volume 59, Issue 2, pp. 190 - 196
OBJECTIVES:We correlated liver and kidney manifestations in a national cohort of patients with autosomal recessive polycystic kidney disease (ARPKD). METHODS:A... 
autosomal recessive polycystic kidney disease | liver disease | combined liver-kidney transplantation | congenital hepatic fibrosis | liver transplantation | ARPKD | SINGLE-CENTER | TRANSPLANTATION | CHILDREN | BILIARY DISEASE | NUTRITION & DIETETICS | CONGENITAL HEPATIC-FIBROSIS | PEDIATRICS | EXPERIENCE | GASTROENTEROLOGY & HEPATOLOGY | ASSOCIATION | PKHD1 MUTATIONS | Liver - pathology | Kidney - pathology | Liver Transplantation - adverse effects | Humans | Child, Preschool | Infant | Male | Esophageal and Gastric Varices - etiology | Esophageal and Gastric Varices - epidemiology | Renal Insufficiency - etiology | Young Adult | Hypertension, Portal - etiology | Polycystic Kidney, Autosomal Recessive - complications | Hypersplenism - epidemiology | Liver Diseases - etiology | Splenomegaly - etiology | Adult | Female | Liver - surgery | Child | Infant, Newborn | Kidney - surgery | Cholangitis - epidemiology | Renal Insufficiency - surgery | Survival Rate | Hepatoblastoma - mortality | Liver Diseases - epidemiology | Biliary Tract - pathology | Cholangitis - etiology | Hypertension, Portal - epidemiology | Hepatoblastoma - surgery | Splenomegaly - epidemiology | Adolescent | Hypersplenism - etiology | Biliary Tract Diseases - etiology | Polycystic Kidney, Autosomal Recessive - surgery | Liver Diseases - surgery | Biliary Tract Diseases - epidemiology | Kidney Transplantation - adverse effects
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6. Full Text Non-cirrhotic portal hypertension – Diagnosis and management
by Khanna, Rajeev and Sarin, Shiv K
Journal of Hepatology, ISSN 0168-8278, 2013, Volume 60, Issue 2, pp. 421 - 441
Summary NCPH is a heterogeneous group of liver disorders of vascular origin, leading to PHT with near normal HVPG. NCPF/IPH is a disorder of young adults or... 
Gastroenterology and Hepatology | Non cirrhotic portal fibrosis | Extrahepatic portal venous obstruction | Portal biliopathy | Portal hypertension | Shunt surgery | POLYCYSTIC KIDNEY-DISEASE | BUDD-CHIARI-SYNDROME | NATURAL-HISTORY | ESOPHAGEAL-VARICES | MINIMAL HEPATIC-ENCEPHALOPATHY | VEIN-THROMBOSIS | NODULAR REGENERATIVE HYPERPLASIA | VENOUS OBSTRUCTION | ENDOSCOPIC SCLEROTHERAPY | TERM FOLLOW-UP | GASTROENTEROLOGY & HEPATOLOGY | Liver Cirrhosis - etiology | Liver Cirrhosis - diagnosis | Esophageal and Gastric Varices - therapy | Humans | Portal Vein - physiopathology | Pancytopenia - diagnosis | Male | Pancytopenia - etiology | Esophageal and Gastric Varices - etiology | Liver Cirrhosis - therapy | Pancytopenia - therapy | Hypertension, Portal - diagnosis | Splenomegaly - diagnosis | Animals | Hypertension, Portal - etiology | Splenomegaly - therapy | Hypertension, Portal - therapy | Splenomegaly - etiology | Female | Hemodynamics | Esophageal and Gastric Varices - diagnosis | Disease Models, Animal | Hypertension | Care and treatment | Diagnosis | Liver cirrhosis
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7. Full Text Spleen Size in Cirrhosis of Different Etiologies
by Kashani, Amir and Salehi, Banafsheh and Anghesom, Deborah and Kawayeh, Anas M and Rouse, Glenn A and Runyon, Bruce A
Journal of Ultrasound in Medicine, ISSN 0278-4297, 02/2015, Volume 34, Issue 2, pp. 233 - 238
Objectives The purpose of this study was to evaluate the impact of cirrhosis etiology on spleen size as measured by sonography and computed tomography (CT).... 
computed tomography | gastrointestinal ultrasound | nonalcoholic fatty liver disease | alcoholic | spleen | hepatitis C | radiography | liver cirrhosis | sonography | Gastrointestinal ultrasound | Radiography | Sonography | Spleen | Computed tomography | Alcoholic | Nonalcoholic fatty liver disease | Hepatitis C | Liver cirrhosis | DIAGNOSIS | LIVER-DISEASE | ESOPHAGEAL-VARICES | ACOUSTICS | SHUNT | HYPERSPLENISM | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | PORTAL-HYPERTENSION | Liver Cirrhosis - etiology | Diagnosis, Differential | Reproducibility of Results | Spleen - diagnostic imaging | Humans | Image Interpretation, Computer-Assisted - methods | Middle Aged | Organ Size | Male | Alcoholism - diagnosis | Splenomegaly - diagnostic imaging | Non-alcoholic Fatty Liver Disease - complications | Hepatitis C - diagnosis | Liver Cirrhosis - diagnostic imaging | Sensitivity and Specificity | Non-alcoholic Fatty Liver Disease - diagnosis | Splenomegaly - etiology | Female | Hepatitis C - complications | Alcoholism - complications | Ultrasonography - methods
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8. Full Text A Sinister Cause of Hematemesis
by Glockenberg, Kati and Weinberg, Ethan M and Wan, David W
Gastroenterology, ISSN 0016-5085, 2015, Volume 148, Issue 3, pp. e5 - e6
Gastroenterology and Hepatology | Hypertension, Portal - etiology | Primary Myelofibrosis - complications | Gastrointestinal Hemorrhage - etiology | Humans | Middle Aged | Splenomegaly - etiology | Hematopoiesis, Extramedullary | Male | Esophageal and Gastric Varices - etiology | Stomach Diseases - etiology | Hematemesis - etiology
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9. Full Text Gaucher disease: haematological presentations and complications
by Thomas, Alison S and Mehta, Atul and Hughes, Derralynn A
British Journal of Haematology, ISSN 0007-1048, 05/2014, Volume 165, Issue 4, pp. 427 - 440
Summary Gaucher disease (GD) is an autosomal recessive lysosomal storage disease, caused by deficiency of the enzyme glucocerebrosidase, required for the... 
glycosphingolipid | Gaucher disease | myeloma | thrombocytopenia | splenomegaly | Thrombocytopenia | Splenomegaly | Myeloma | Glycosphingolipid | MULTIPLE-MYELOMA | PLATELET-FUNCTION | VELAGLUCERASE ALPHA | NATURAL-HISTORY | N-BUTYLDEOXYNOJIRIMYCIN | GENE-FREQUENCIES | UNDETERMINED SIGNIFICANCE | MONOCLONAL GAMMOPATHY | COAGULATION ABNORMALITIES | HEMATOLOGY | ENZYME REPLACEMENT THERAPY | Glucosylceramidase - genetics | Humans | Lewy Body Disease - enzymology | Gaucher Disease - blood | Gaucher Disease - therapy | Splenectomy | 1-Deoxynojirimycin - therapeutic use | Lewy Body Disease - genetics | Lysosomes - metabolism | Splenomegaly - etiology | 1-Deoxynojirimycin - analogs & derivatives | Gaucher Disease - physiopathology | Lysosomes - pathology | Anemia - etiology | Gaucher Disease - enzymology | Enzyme Replacement Therapy | Genetic Predisposition to Disease | Thrombocytopenia - etiology | Combined Modality Therapy | Inflammation | Gaucher Disease - complications | Parkinson Disease - genetics | Unfolded Protein Response | Macrophage Activation | Multiple Myeloma - etiology | Parkinson Disease - enzymology | Glucosylceramidase - physiology | Glycosphingolipids - metabolism | Hemorrhagic Disorders - etiology | Disease Management | Gaucher Disease - classification
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10. Full Text Adult Acute Leukemia
by Cornell, Robert Frank, MD and Palmer, Jeanne, MD
Disease-a-Month, ISSN 0011-5029, 2012, Volume 58, Issue 4, pp. 219 - 238
Internal Medicine | MEDICINE, GENERAL & INTERNAL | PROGNOSTIC-FACTORS | ACUTE LYMPHOBLASTIC-LEUKEMIA | ACUTE MYELOGENOUS LEUKEMIA | HIGH-DOSE CYTARABINE | ACUTE MYELOID-LEUKEMIA | TRANS-RETINOIC ACID | STEM-CELL TRANSPLANTATION | 1ST COMPLETE REMISSION | WORLD-HEALTH-ORGANIZATION | ACUTE PROMYELOCYTIC LEUKEMIA | Translocation, Genetic | Prognosis | Age Factors | Proto-Oncogene Proteins c-ets - genetics | Humans | Antineoplastic Agents - therapeutic use | Leukemia, Myeloid, Acute - etiology | fms-Like Tyrosine Kinase 3 - genetics | Diploidy | Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy | Splenomegaly - etiology | Adult | Leukocyte Count | CCAAT-Enhancer-Binding Proteins - genetics | Nuclear Proteins - genetics | Anemia - etiology | Leukemia, Myeloid, Acute - therapy | Leukemia, Promyelocytic, Acute - therapy | Leukostasis - etiology | Spinal Puncture | Thrombocytopenia - etiology | Risk Factors | Leukemia, Promyelocytic, Acute - etiology | Hematopoietic Stem Cell Transplantation | Repressor Proteins - genetics | Pancytopenia - etiology | Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis | Leukemia, Myeloid, Acute - diagnosis | Disseminated Intravascular Coagulation - etiology | Protein Kinase Inhibitors - therapeutic use | Leukemia, Promyelocytic, Acute - classification | Leukemia, Promyelocytic, Acute - diagnosis | Lymphatic Diseases - etiology | Mutation | Precursor Cell Lymphoblastic Leukemia-Lymphoma - etiology | Core Binding Factor Alpha 2 Subunit - genetics | Karyotype | Leukemia, Myeloid, Acute - classification | Precursor Cell Lymphoblastic Leukemia-Lymphoma - classification | Hepatomegaly - etiology
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11. Full Text An Egyptian family with H syndrome due to a novel mutation in SLC29A3 illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin‐dependent diabetes and Faisalabad histiocytosis
by Elbarbary, Nancy S and Tjora, Erling and Molnes, Janne and Lie, Benedicte A and Habib, Mohammad A and Salem, Mona A and Njølstad, Pål Rasmus
Pediatric Diabetes, ISSN 1399-543X, 09/2013, Volume 14, Issue 6, pp. 466 - 472
The SLC29A3 gene, encoding hENT3, a member of the equilibrative nucleoside transporter family, has recently been found mutated in Faisalabad histiocytosis,... 
mutation | gene | syndrome | diabetes | Diabetes | Mutation | Gene | Syndrome | Humans | Genetic Diseases, Inborn - genetics | Hyperpigmentation - etiology | Male | Nucleoside Transport Proteins - metabolism | Young Adult | Diabetes Mellitus, Type 1 - etiology | Splenomegaly - etiology | Adult | Female | Genetic Diseases, Inborn - metabolism | Siblings | Histiocytosis - etiology | Hypertrophy, Left Ventricular - etiology | Nucleoside Transport Proteins - genetics | Homozygote | Hearing Loss, Sensorineural - etiology | Adolescent | Consanguinity | Genetic Diseases, Inborn - physiopathology | Lymphatic Diseases - etiology | Contracture - etiology | Hepatomegaly - etiology | Genetic research | Skin diseases | Genetic aspects | Histiocytosis | Insulin
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12. Full Text The spleen and sickle cell disease: the sick(led) spleen
by Brousse, Valentine and Buffet, Pierre and Rees, David
British Journal of Haematology, ISSN 0007-1048, 07/2014, Volume 166, Issue 2, pp. 165 - 176
Summary The spleen has a combined function of immune defence and quality control of senescent or altered red cells. It is the first organ injured in sickle... 
acute splenic sequestration | hyposplenism | childhood | spleen | sickle cell disease | Hyposplenism | Spleen | Sickle cell disease | Acute splenic sequestration | Childhood | UNITED-STATES | HEMOGLOBIN SC DISEASE | RISK-FACTORS | PULMONARY-HYPERTENSION | C DISEASE | IMPROVED SURVIVAL | MEMORY B-CELLS | HEMATOLOGY | YOUNG-CHILDREN | FUNCTIONAL ASPLENIA | Disease Susceptibility | Anemia, Sickle Cell - complications | Humans | Splenic Diseases - etiology | Hypersplenism - etiology | Splenic Diseases - therapy | Splenomegaly - etiology | Atrophy - etiology | Spleen - physiology | Spleen - pathology | Opportunistic Infections - complications | Sickle cell anemia
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