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Cross-Reactivity Wikipedia

The American Journal of Tropical Medicine and Hygiene . 71 (3): 297–305. doi : 10.4269/ajtmh.2004.71.297 . PMID 15381810 . ^ Mandelboim M, Bromberg M, Sherbany H, Zucker I, Yaary K, Bassal R, et al.
Aleutian Disease Wikipedia

Parvoviridae > Parvovirinae > Amdoparvovirus > Carnivore amdoparvovirus 1 ^ Canuti M, Whitney HG, Lang AS (2015). "Amdoparvoviruses in small mammals: expanding our understanding of parvovirus diversity, distribution, and pathology" . ... PMID 19961696 . ^ ELIMINATION OF PATHOGENIC INFECTION IN FARMED ANIMAL POPULATIONS ^ Canuti M, O'Leary KE, Hunter BD, Spearman G, Ojkic D, Whitney HG, Lang AS (January 2016).

PTPN11, IVNS1ABP
Aminolevulinic Acid Dehydratase Deficiency Porphyria Wikipedia

ISBN 978-1-4160-2999-1 . ^ a b c d e f g h i j k l m n o "ALAD-Deficiency Porphyria (ADP)" . ... PMC 1785348 . PMID 17236137 . ^ Doss M, von Tiepermann R, Schneider J, Schmid H (October 1979).

ALAD, HMBS, CPOX, FECH, UROD, CYP2B6, PPOX
- Hepatic Porphyria Wikipedia
  
  Hepatic porphyria Specialty Endocrinology Hepatic porphyrias is a form of porphyria in which toxic porphyrin molecules build up in the liver . Hepatic porphyrias can result from a number of different enzyme defiencies. [1] Examples include (in order of synthesis pathway): Acute intermittent porphyria Porphyria cutanea tarda and Hepatoerythropoietic porphyria Hereditary coproporphyria Variegate porphyria See also [ edit ] Erythropoietic porphyria References [ edit ] ^ "OMIM - PORPHYRIA, CONGENITAL ERYTHROPOIETIC" . Retrieved 2008-12-04 . External links [ edit ] Classification D ICD - 10 : E80 ICD - 9-CM : 277.1 MeSH : D017094 Porphyrias,+Hepatic at the US National Library of Medicine Medical Subject Headings (MeSH) www.drugs-porphyria.com www.porphyria-europe.com v t e Heme metabolism disorders Porphyria , hepatic and erythropoietic ( porphyrin ) early mitochondrial: ALAD porphyria Acute intermittent porphyria cytoplasmic: Gunther disease/congenital erythropoietic porphyria Porphyria cutanea tarda / Hepatoerythropoietic porphyria late mitochondrial: Hereditary coproporphyria Harderoporphyria Variegate porphyria Erythropoietic protoporphyria Hereditary hyperbilirubinemia ( bilirubin ) unconjugated: Gilbert's syndrome Crigler–Najjar syndrome Lucey–Driscoll syndrome conjugated: Dubin–Johnson syndrome nd sheet Rotor syndrome This article about an endocrine, nutritional, or metabolic disease is a stub . You can help Wikipedia by expanding it . v t e
Caustic Ingestion Wikipedia

Caustic ingestions in adults usually involve larger amounts of ingested material during attempts of self harm. [1] Due to the greater amount of material usually ingested; injuries are often more severe in the intentional ingestions of adolescents and adults as compared to those of children. [1] Commonly ingested substances include ammonium hydroxide (found in general cleaner and grease remover), sodium hydroxide or potassium hydroxide (found in drain opener or oven cleaner), sodium hypochlorite (bleach), oxalic acid (metal polish) and hydrochloric acid (toilet bowl cleaner). [1] Storage of caustic substances in water or drink containers is a risk factor for accidental ingestion of these materials, particularly in children. [2] Boys of preschool age are at the greatest risk of accidental caustic ingestion. [3] Prevention [ edit ] Preventative measures have been recommended that are intended to decrease the risk of accidental ingestion of caustic substances including": [3] Keeping caustic substances in locked cabinets or on upper shelves Not storing chemical substances in food or drink containers Not keeping large amounts of detergent in the home Not mentioning a drug as "candy" when giving it as medication Keeping the phone number for poison control in the home Keeping caustic substances in labelled containers References [ edit ] ^ a b c d e f g h i j k l m n o p q r s Longo, Dan L.; Hoffman, Robert S.; Burns, Michele M.; Gosselin, Sophie (30 April 2020).
Periapical Granuloma Wikipedia

ISBN 9781437726077 . ^ a b Fernandes M, de Ataide I (October 2010). "Nonsurgical management of periapical lesions" . ... The Journal of the Stomatological Society, Japan . 72 (1): 13–8. doi : 10.5357/koubyou.71and72.13 . PMID 15856767 . ^ Fernandes M, De Ataide I (June 2010). "Non-surgical management of a large periapical lesion using a simple aspiration technique: a case report".

TNF, MMP9, TNFRSF11B, TNFSF11, FOXP3, SIRT1, IL1B, VEGFA, NOS2, PTGS2, CXCL11, TGFB1, BTF3P11, VIP, TP63, HSPB3, CD163, PDPN, SIRT2, B3GAT1, MMP13, MMP2, CD8A, HSPB2, CD34, CD79A, CEACAM8, CCR5, EP300, FOXO3, HSPB1, ICAM1, MMP1, IFNG, IL1A, IL2RG, IL17A, ITGA4, LGALS1, MDK, IL33
Melanocytoma Wikipedia

.; Steinmetz, Robert L.; Craythorn, Judy M.; Loftfield, Katherine; Gieser, Stephen C.; Brady, Steven E. (1985). ... ISSN 0039-6257 . PMID 3992470 . ^ P. M. Sharma u. a.: Malignant transformation of optic disc melanocytoma?
Mirizzi's Syndrome Wikipedia

Mirizzi specialized in abdominal and thoracic surgery and would write prolifically on related surgical topics. [6] [7] References [ edit ] ^ a b Vitale M. Mirizzi Syndrome Type IV: An Atypical Presentation That Is Difficult to Diagnose Preoperatively. 2009. ... Neela Lamki; Bernard D Coombs; Abraham H Dachman; Robert M Krasny; John Karani (eds.). "Mirizzi syndrome" . eMedicine .

AZU1, HDLBP, SLBP, STAM2, HEBP1, BTBD8
- Mirizzi Syndrome Orphanet
  
  A rare biliary tract disease characterized by external compression and subsequent obstruction of an extrahepatic biliary duct by one or more gallstones in the cystic duct or the gallbladder. Patients may present with acute or chronic cholecystitis with right upper abdominal pain, nausea, and vomiting, jaundice, or cholangitis. Cholecystobiliary or -enteric fistulae can arise due to chronic inflammation and ulceration.
Sweet Itch Wikipedia

Trisciuoglio (2006) "Equine Culicoides Hypersensitivity: Evaluation of a Skin Test and of Humoral Response", Journal of Veterinary Medicine , Series A 53 (1), 30–33 ^ Langner, KFA, Darpel, KE, Denison, E, Drolet, BS, Leibold, W, Mellor, PS, Mertens, PPC, Nimtz, M, Greiser-Wilke, I, (2007) "Collection and Analysis of Salivary Proteins from the Biting Midge Culicoides nubeculosus (Diptera: Ceratopogonidae)", Journal of Medical Entomology , Volume 44, Number 2, March 2007, pp. 238-248(11) ^ A. P. Foster, J. McKelvie, and F. M. Cunningham (1998) "Inhibition of antigen-induced cutaneous responses of ponies with insect hypersensitivity by the histamine-1 receptor antagonist chlorpheniramine ", The Veterinary Record , Vol 143, Issue 7, 189-193 ^ Animal Health TrustEquine Clinics ^ PT Colahan, IG Mayhew, AM Merrit & JN Moore, Manual of Equine Medicine and Surgery, Copyright Mosby Inc (1999) (pp. 474-475) ^ PT Colahan, IG Mayhew, AM Merrit & JN Moore, Manual of Equine Medicine and Surgery, Copyright Mosby Inc (1999) (pp. 474) ^ J Littlewood (1999) "Control of ectoparasites in horses", In Practice (BVA Publications Ltd) 21: 418-424 ^ PT Colahan, IG Mayhew, AM Merrit & JN Moore, Manual of Equine Medicine and Surgery, Copyright Mosby Inc (1999) (p. 475) ^ RR Pascoe, DC Knottenbelt, Manual of Equine Dermatology Published 1999, Elsevier Health Sciences (p. 131) ^ Friberg, Logas (1999) "Treatment of Culicoides hypersensitive horses with high-dose n-3 fatty acids: a double-blinded crossover study" Veterinary Dermatology 10 (2), 117–122 ^ PT Colahan, IG Mayhew, AM Merrit & JN Moore, Manual of Equine Medicine and Surgery, Copyright Mosby Inc (1999) (p. 475) ^ RJ Rose & DR Hodgson, Manual of Equine Practice Copyright WB Saunders (2000) (p. 482) ^ The Holistic Horse PonyGalaxy Detailed Information On SSRD External links [ edit ] British Horse Society Sweet Itch Datasheet Detailed Information on Sweet Itch and its Causes Information about what Sweet Itch is, Causes and Treatment The Sweet Itch Help Centre
Plexiform Angiomyxoid Myofibroblastic Tumor Wikipedia

.; Chmelar, C.; Höhler, T.; Agaimy, A.; Vieth, M. (2012-01-29). "Plexiformer angiomyxoider myofibroblastischer Tumor des Magens". ... PMID 20498030 . ^ Duckworth, Lizette Vila; Gonzalez, Raul S.; Martelli, Matthew; Liu, Chen; Coffin, Cheryl M.; Reith, John D. (January 2014). "Plexiform Fibromyxoma: Report of Two Pediatric Cases and Review of the Literature".
Fragmentation Of Memory Wikipedia

CiteSeerX 10.1.1.1025.9891 . doi : 10.1002/acp.950 . ^ a b c d e f Bedard-Gilligan, M.; Zoellner, L. A. (2012). "Dissociation and Memory Fragmentation in Posttraumatic Stress Disorder: An Evaluation of the Dissociative Encoding Hypothesis" . ... German Life & Letters . 61 (2): 215–230. doi : 10.1111/j.1468-0483.2008.00420.x . ^ Candel, I.; Merckelbach, H.; Kuijpers, M. (2003). "Dissociative experiences are related to commissions in emotional memory" .
Maternal Near Miss Wikipedia

Identification criteria [ edit ] According to the World Health Organization, if a woman presents any of the conditions below during pregnancy, childbirth or within 42 days of termination of pregnancy and survives, she is considered as a maternal near miss case. [10] Cardiovascular dysfunction a) Shock b) Cardiac Arrest c) Severe hypoperfusion (lactate >5 mmol/L or >45 mg/dL) d) Severe acidosis (pH<7.1) e) Use of continuous vasoactive drugs f) Cardio-pulmonary resuscitation Respiratory dysfunction g) Acute cyanosis h) Gasping i) Severe tachypnea (respiratory rate>40 breaths per minute) j) Severe bradypnea (respiratory rate<6 breaths per minute) k) Severe hypoxemia (O2 saturation <90% for ≥60min or PAO2/FiO2<200) l) Intubation and ventilation not related to anaesthesia Renal dysfunction m) Oliguria non responsive to fluids or diuretics n) Severe acute azotemia (creatinine >300 μmol/ml or >3.5 mg/dL) o) Dialysis for acute renal failure Coagulation dysfunction p) Failure to form clots q) Severe acute thrombocytopenia (<50,000 platelets/ml) r) Massive transfusion of blood or red cells (≥ 5 units) Hepatic dysfunction s) Jaundice in the presence of pre-eclampsia t) Severe acute hyperbilirubinemia (bilirubin>100 μmol/L or >6.0 mg/dL) Neurologic dysfunction u) Prolonged unconsciousness or coma (lasting >12 hours) v) Stroke w) Uncontrollable fit / status epilepticus x) Global paralysis Uterine dysfunction y) Hysterectomy due to uterine infection or haemorrhage Sources [ edit ] Adisasmita, Asri; et al. (2008). ... PMC 2311270 . PMID 18366625 . Dott, M; N . Orakail; H . Ebadi; F . Hernandez; K .
Fungal Pneumonia Wikipedia

Retrieved 14 February 2013 . ^ Morrell M, Fraser VJ, Kollef MH (September 2005). ... "Webinar on fungal diagnostics" (PDF) . ^ , Philippe Hauser, Lagrou K, Cui X, PerlinD S, Park S, Harrison E, Meerssman W, Hughes M J, Bowyer P, Denning DW, Bille J, Lass-Flor C, Maertens J.

TNF, GATA2, IL13, NOS2, CHIT1, PTX3, TREM1, CLEC6A, CD200R1
Schistocyte Wikipedia

.; d’ONOFRIO, G.; BRIGGS, C.; ERBER, W.; JOU, J. M.; LEE, S. H.; McFADDEN, S.; VIVES-CORRONS, J. ... PMID 5412670 . ^ Lesesve, J; Martin, M; Banasiak, C; Andre-Kerneis, E; Bardet, V; Lusina, D; Kharbach, A; Genevieve, F; Lecompte, T (2014).
Chorionic Hematoma Wikipedia

Infante; U. Menakaya; I. Casikar; S. Reid; M. Mongelli; G. Condous (2013). "OP03.03: Does the presence of subchorionic haematoma increase the risk of miscarriage?" ... Ultrasound in Obstetrics & Gynecology . 42 (s1): 54. doi : 10.1002/uog.12736 . ^ Maso, G.; Dʼottavio, G.; De Seta, F.; Sartore, A.; Piccoli, M.; Mandruzzato, G. (2005). "First-Trimester Intrauterine Hematoma and Outcome of Pregnancy".
Kikuchi Disease Wikipedia

Retrieved 17 April 2018 . ^ Kikuchi M. Lymphadenitis showing focal reticulum cell hyperplasia with nuclear debris and phagocytes. ... W.; Hasserjian, R. P.; McClain, C. M.; Wang, B; Mosse, C. A. (2013). "Kikuchi-Fujimoto lymphadenitis: Role of parvovirus B-19, Epstein-Barr virus, human herpesvirus 6, and human herpesvirus 8".

BCL2, CASP3, TNFRSF8, EXT1, GBP1, GZMB, HLA-DPA1, HLA-DPB1, IFI27, IL3RA, CXCL10, MPO, TRBV20OR9-2, PDLIM7
- Kikuchi-Fujimoto Disease Orphanet
  
  Kikuchi-Fujimoto disease (KFD) is a benign and self-limited disorder, characterized by regional cervical lymphadenopathy with tenderness, usually accompanied with mild fever and night sweats. Less frequent symptoms include weight loss, nausea, vomiting, sore throat. Epidemiology Kikuchi-Fujimoto disease is an extremely rare disease known to have a worldwide distribution with higher prevalence among Japanese and other Asiatic individuals. Prevalence is unknown. Only isolated cases are reported in Europe. Etiology The clinical, histopathological and immunohistochemical features appear to point to a viral etiology, a hypothesis that still has not been proven. Diagnostic methods KFD is generally diagnosed on the basis of an excisional biopsy of affected lymph nodes.
- Kikuchi Disease Gard
  
  Kikuchi disease is a benign (non-cancerous) condition of the lymph nodes. The main symptoms include swollen lymph nodes in the neck, mild fever , and night sweats . Less common symptoms include weight loss, nausea, vomiting, and sore throat. While the exact cause of this condition is unknown, infectious and autoimmune causes have been suggested. Kikuchi disease usually gets better (resolves) on its own within one to four months (although it may take up to a year), with or without treatment.
Multisystem Developmental Disorder Wikipedia

Cutis; cutaneous medicine for the practitioner . 57 (5): 346–8. PMID 8726717 . ^ Melekos, M; Barbalias, G; Asbach, HW (1987). ... ISBN 9780801882128 . ^ Kaduthodil, M; Prasad, D; Lowe, A; Punekar, A; et al. (2012).
Pseudomonas Infection Wikipedia

External links [ edit ] Classification D ICD - 10 : B96.5, J15.1, P23.5 ICD - 9-CM : 041.7 , 482.1 MeSH : D011552 v t e Proteobacteria -associated Gram-negative bacterial infections α Rickettsiales Rickettsiaceae / ( Rickettsioses ) Typhus Rickettsia typhi Murine typhus Rickettsia prowazekii Epidemic typhus , Brill–Zinsser disease , Flying squirrel typhus Spotted fever Tick-borne Rickettsia rickettsii Rocky Mountain spotted fever Rickettsia conorii Boutonneuse fever Rickettsia japonica Japanese spotted fever Rickettsia sibirica North Asian tick typhus Rickettsia australis Queensland tick typhus Rickettsia honei Flinders Island spotted fever Rickettsia africae African tick bite fever Rickettsia parkeri American tick bite fever Rickettsia aeschlimannii Rickettsia aeschlimannii infection Mite-borne Rickettsia akari Rickettsialpox Orientia tsutsugamushi Scrub typhus Flea-borne Rickettsia felis Flea-borne spotted fever Anaplasmataceae Ehrlichiosis : Anaplasma phagocytophilum Human granulocytic anaplasmosis , Anaplasmosis Ehrlichia chaffeensis Human monocytotropic ehrlichiosis Ehrlichia ewingii Ehrlichiosis ewingii infection Rhizobiales Brucellaceae Brucella abortus Brucellosis Bartonellaceae Bartonellosis : Bartonella henselae Cat-scratch disease Bartonella quintana Trench fever Either B. henselae or B. quintana Bacillary angiomatosis Bartonella bacilliformis Carrion's disease , Verruga peruana β Neisseriales M+ Neisseria meningitidis/meningococcus Meningococcal disease , Waterhouse–Friderichsen syndrome , Meningococcal septicaemia M− Neisseria gonorrhoeae/gonococcus Gonorrhea ungrouped: Eikenella corrodens / Kingella kingae HACEK Chromobacterium violaceum Chromobacteriosis infection Burkholderiales Burkholderia pseudomallei Melioidosis Burkholderia mallei Glanders Burkholderia cepacia complex Bordetella pertussis / Bordetella parapertussis Pertussis γ Enterobacteriales ( OX− ) Lac+ Klebsiella pneumoniae Rhinoscleroma , Pneumonia Klebsiella granulomatis Granuloma inguinale Klebsiella oxytoca Escherichia coli : Enterotoxigenic Enteroinvasive Enterohemorrhagic O157:H7 O104:H4 Hemolytic-uremic syndrome Enterobacter aerogenes / Enterobacter cloacae Slow/weak Serratia marcescens Serratia infection Citrobacter koseri / Citrobacter freundii Lac− H2S+ Salmonella enterica Typhoid fever , Paratyphoid fever , Salmonellosis H2S− Shigella dysenteriae / sonnei / flexneri / boydii Shigellosis , Bacillary dysentery Proteus mirabilis / Proteus vulgaris Yersinia pestis Plague / Bubonic plague Yersinia enterocolitica Yersiniosis Yersinia pseudotuberculosis Far East scarlet-like fever Pasteurellales Haemophilus : H. influenzae Haemophilus meningitis Brazilian purpuric fever H. ducreyi Chancroid H. parainfluenzae HACEK Pasteurella multocida Pasteurellosis Actinobacillus Actinobacillosis Aggregatibacter actinomycetemcomitans HACEK Legionellales Legionella pneumophila / Legionella longbeachae Legionnaires' disease Coxiella burnetii Q fever Thiotrichales Francisella tularensis Tularemia Vibrionaceae Vibrio cholerae Cholera Vibrio vulnificus Vibrio parahaemolyticus Vibrio alginolyticus Plesiomonas shigelloides Pseudomonadales Pseudomonas aeruginosa Pseudomonas infection Moraxella catarrhalis Acinetobacter baumannii Xanthomonadaceae Stenotrophomonas maltophilia Cardiobacteriaceae Cardiobacterium hominis HACEK Aeromonadales Aeromonas hydrophila / Aeromonas veronii Aeromonas infection ε Campylobacterales Campylobacter jejuni Campylobacteriosis , Guillain–Barré syndrome Helicobacter pylori Peptic ulcer , MALT lymphoma , Gastric cancer Helicobacter cinaedi Helicobacter cellulitis

DCTN4, CRP, CFTR, ELANE, IMPA1, MIF, PRTN3, RAC2, SLC9A3, SLPI, TNF, VIM, BRAP, TNFSF13B, SMOX, FLG2
Myxoid Liposarcoma Wikipedia

Bibcode : 1993Natur.363..640C . doi : 10.1038/363640a0 . PMID 8510758 . ^ Forni C, Minuzzo M, Virdis E, et al. (February 2009). ... Genes Chromosomes Cancer . 5 (4): 278–85. doi : 10.1002/gcc.2870050403 . PMID 1283316 . ^ Göransson M, Andersson MK, Forni C, et al. (January 2009).

DDIT3, FUS, EWSR1, CD6, PIK3CA, MDM2, LOC110806263, CTAG1B, CTAG1A, MVP, PIK3CB, LRP1, PIK3CG, HCCS, GLI1, TP53, PIK3CD, TERT, CREB3L2, PRG4, ERG, PTPRA, CDK4, ATF1, RPSA, NR4A3, THPO, WNT1, VIM, HMGA2, ZEB1, SYT1, FGF23, EBP, TAF15, CLDN6, CIB1, SSX2, PRAME, SMUG1, INTS1, CTAG2, ZNF654, ANKRD36B, PDIK1L, MIR135B, MXLPO, SS18, AKT1, S100B, S100A1, CD34, CDKN1B, CDKN2A, E2F1, ERCC5, FGFR2, FLT1, MTOR, GDNF, HMGA1, HSP90AA1, HTC2, IGF1, IGF1R, IL4R, MAD2L1, MAGEA3, MXI1, MYC, NNAT, SERPINE1, PGF, ALK, PLAG1, PMAIP1, PML, PPARG, H3P10
- Myxoid/round Cell Liposarcoma Orphanet
  
  Myxoid/round cell liposarcoma (MRCLS) is a type of liposarcoma (LS; see this term) mostly located in the limbs, with a variable behavior depending on the histological subtype. Both myxoid and round cell are distinct histological subtypes of LS. Epidemiology The incidence is approximately 1/769, 000 per year and it accounts for 30% or less of all LS cases. Clinical description MRCLS presents at a younger age than other LS subtypes with typical age of diagnosis ranging from 35-55 years. It predominantly occurs in the limbs (most frequently in the thighs) and rarely arises in the retroperitoneum or subcutaneous tissue. One third of MRCLS cases will become metastatic with tumors spreading to unusual bone and soft tissue locations with multifocal synchronous or metachronous spread to fat pad areas in the retroperitoneum, trunk, pericardium and axilla.
- Myxoid Liposarcoma Omim
  
  A number sign (#) is used with this entry because myxoid liposarcoma can be caused by chromosomal translocations, most commonly t(12;16)(q13;p11) (Panagopoulos et al., 1996). Description Myxoid liposarcoma is a soft tissue tumor that tends to occur in the limbs (especially the thigh) of patients ranging in age from 35 to 55 years. It is defined by the presence of a hypocellular spindle cell proliferation set in a myxoid background, often with mucin pooling. Lipoblasts tend to be small and often monovacuolated and to cluster around vessels or at the periphery of the lesion (review by Dei Tos, 2000). Cytogenetics Limon et al. (1986) and Turc-Carel et al. (1986) described a specific chromosome change, t(12;16)(q13;p11), in the tumors of all 4 cases of myxoid liposarcoma studied.
- Myxoid Liposarcoma Gard
  
  Myxoid liposarcoma is a subtype of liposarcoma , tumors that arise in the body’s fat tissue. Other categories of liposarcoma include well-differentiated; dedifferentiated; round cell; and pleomorphic.[1] Round cell and myxoid liposarcomas are sometimes grouped together into one category known as myxoid/round cell liposarcoma (MRCLS).[2] In adults, liposarcomas are the most common type of soft tissue sarcoma. The cause of liposarcomas is not well-established but trauma has been implicated in some cases. Myxoid liposarcomas generally arise in the lower extremities. Symptoms may vary depending on the location of the tumor but may include swelling; decreased range of motion; numbness; fatigue; abdominal pain; weight loss; nausea; and vomiting. Many patients with liposarcoma have no symptoms until the tumor is large and interferes with neighboring structures.
Acne Conglobata Wikipedia

Alternatively, nodules can be injected with corticosteroids such as triamcinolone . [8] See also [ edit ] List of cutaneous conditions References [ edit ] ^ Freedberg, Irwin M.; Eisen, Arthur Z.; Wolff, Klaus; Austen, K. ... PMC 4228650 . PMID 25396138 . ^ Shirakawa M, Uramoto K, Harada FA (August 2006).

TLR4
Fibrolamellar Hepatocellular Carcinoma Wikipedia

. ^ Dinh TA, Vitucci EC, Wauthier E, Graham RP, Pitman WA, Oikawa T, Chen M, Silva G, Greene KG, Torbenson MS, Reid LM, Sethupathy P (2017) Comprehensive analysis of The Cancer Genome Atlas reveals a unique gene and non-coding RNA signature of fibrolamellar carcinoma. ... AMA J Dis Child 91(2):168–186 ^ Craig JR, Peters RL, Edmondson HA, Omata M. Fibrolamellar carcinoma of the liver: a tumor of adolescents and young adults with distinctive clinico-pathologic features.

PRKACA, DNAJB1, EGFR, NTS, TP53, DNAJA2, SDC1, HNF1A, TPT1, PAX8, NR0B2, DNAJB6, YAP1, PRKCA, IGF2BP1, RASSF1, CD274, CLPTM1L, GLIS2, DNAJC14, LINC00473, GLIS1, GLIS3, BRD2, APC, PRKAR1A, FGFR1, ARAF, CCND1, CBFA2T3, CD68, CDH1, CTNNB1, CYP19A1, ERBB2, FGFR2, APRT, HSPA4, KRAS, KRT19, MB, MDM4, MFAP1, NFYA, PDCD1, DNAJB1P1
- Fibrolamellar Carcinoma Gard
  
  Fibrolamellar carcinoma (FLC) is a rare form of liver cancer which is generally diagnosed in adolescents and young adults (before age 40). Many people with early FLC have no signs or symptoms of the condition. When present, symptoms are often nonspecific (i.e. abdominal pain, weight loss, malaise ) and blamed on other, more common conditions. The exact underlying cause of FLC is poorly understood. Unlike other forms of liver cancer, FLC typically occurs in the absence of underlying liver inflammation or scarring; thus, specific risk factors for this condition remain unidentified. FLC is typically treated with surgical resection .
- Fibrolamellar Hepatocellular Carcinoma Orphanet
  
  A rare variant of hepatocellular carcinoma (HCC) presenting in adolescents or young adults with no underlying liver disease. Clinical presentation is non specific, with abdominal mass, abdominal discomfort or pain, fatigue and weight loss. Patients can also be asymptomatic. HCC markers (alpha fetoprotein) are normal. Fibrolamellar HCC presents as a unique, well-delimited mass at imagery and a biopsy confirms the diagnosis, showing well-differentiated tumor cells surrounded by thick collagen bands.