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Granuloma Annulare In Hiv Disease
Wikipedia
ISBN 978-0-7216-2921-6 . v t e Cutaneous keratosis, ulcer, atrophy, and necrobiosis Epidermal thickening keratoderma : Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis : Seborrheic keratosis Clonal seborrheic keratosis Common seborrheic keratosis Irritated seborrheic keratosis Seborrheic keratosis with squamous atypia Reticulated seborrheic keratosis Dermatosis papulosa nigra Keratosis punctata of the palmar creases other hyperkeratosis : Acanthosis nigricans Confluent and reticulated papillomatosis Callus Ichthyosis acquisita Arsenical keratosis Chronic scar keratosis Hyperkeratosis lenticularis perstans Hydrocarbon keratosis Hyperkeratosis of the nipple and areola Inverted follicular keratosis Lichenoid keratosis Multiple minute digitate hyperkeratosis PUVA keratosis Reactional keratosis Stucco keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: Keloid Hypertrophic scar Cutis verticis gyrata Necrobiosis / granuloma Necrobiotic/palisading Granuloma annulare Perforating Generalized Subcutaneous Granuloma annulare in HIV disease Localized granuloma annulare Patch-type granuloma annulare Necrobiosis lipoidica Annular elastolytic giant-cell granuloma Granuloma multiforme Necrobiotic xanthogranuloma Palisaded neutrophilic and granulomatous dermatitis Rheumatoid nodulosis Interstitial granulomatous dermatitis / Interstitial granulomatous drug reaction Foreign body granuloma Beryllium granuloma Mercury granuloma Silica granuloma Silicone granuloma Zirconium granuloma Soot tattoo Tattoo Carbon stain Other/ungrouped eosinophilic dermatosis Granuloma faciale Dermis / localized CTD Cutaneous lupus erythematosus chronic: Discoid Panniculitis subacute : Neonatal ungrouped: Chilblain Lupus erythematosus–lichen planus overlap syndrome Tumid Verrucous Rowell's syndrome Scleroderma / Morphea Localized scleroderma Localized morphea Morphea–lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma Atrophic / atrophoderma Lichen sclerosus Anetoderma Schweninger–Buzzi anetoderma Jadassohn–Pellizzari anetoderma Atrophoderma of Pasini and Pierini Acrodermatitis chronica atrophicans Semicircular lipoatrophy Follicular atrophoderma Linear atrophoderma of Moulin Perforating Kyrle disease Reactive perforating collagenosis Elastosis perforans serpiginosa Perforating folliculitis Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum / Pseudo-ainhum v t e Medicine Specialties and subspecialties Surgery Cardiac surgery Cardiothoracic surgery Colorectal surgery Eye surgery General surgery Neurosurgery Oral and maxillofacial surgery Orthopedic surgery Hand surgery Otolaryngology ENT Pediatric surgery Plastic surgery Reproductive surgery Surgical oncology Transplant surgery Trauma surgery Urology Andrology Vascular surgery Internal medicine Allergy / Immunology Angiology Cardiology Endocrinology Gastroenterology Hepatology Geriatrics Hematology Hospital medicine Infectious disease Nephrology Oncology Pulmonology Rheumatology Obstetrics and gynaecology Gynaecology Gynecologic oncology Maternal–fetal medicine Obstetrics Reproductive endocrinology and infertility Urogynecology Diagnostic Radiology Interventional radiology Nuclear medicine Pathology Anatomical Clinical pathology Clinical chemistry Cytopathology Medical microbiology Transfusion medicine Other Addiction medicine Adolescent medicine Anesthesiology Dermatology Disaster medicine Diving medicine Emergency medicine Mass gathering medicine Family medicine General practice Hospital medicine Intensive care medicine Medical genetics Narcology Neurology Clinical neurophysiology Occupational medicine Ophthalmology Oral medicine Pain management Palliative care Pediatrics Neonatology Physical medicine and rehabilitation PM&R Preventive medicine Psychiatry Addiction psychiatry Radiation oncology Reproductive medicine Sexual medicine Sleep medicine Sports medicine Transplantation medicine Tropical medicine Travel medicine Venereology Medical education Medical school Bachelor of Medicine, Bachelor of Surgery Bachelor of Medical Sciences Master of Medicine Master of Surgery Doctor of Medicine Doctor of Osteopathic Medicine MD–PhD Related topics Alternative medicine Allied health Dentistry Podiatry Pharmacy Physiotherapy Molecular oncology Nanomedicine Personalized medicine Public health Rural health Therapy Traditional medicine Veterinary medicine Physician Chief physician History of medicine Book Category Commons Wikiproject Portal Outline This cutaneous condition article is a stub .
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Papular Mucinosis
Wikipedia
If viscera is involved, the disease will be fatal. The dermatoneuro syndrome is a rare neurological complication of the disease presenting with fever, seizures and altered mental status. ... External links [ edit ] Classification D ICD - 10 : L98.5 ICD - 9-CM : 701.8 MeSH : D053718 External resources eMedicine : article/1074545 v t e Mucinosis / Lichen myxedematosus Localized lichen myxedematosus Discrete papular lichen myxedematosus Acral persistent papular mucinosis Self-healing papular mucinosis / Self-healing juvenile cutaneous mucinosis Papular mucinosis of infancy Atypical lichen myxedematosus Atypical tuberous myxedema Nodular lichen myxedematosus Other primary mucinoses Cutaneous focal mucinosis Cutaneous lupus mucinosis Eccrine mucinosis Alopecia mucinosa Perifollicular mucinosis Stiff skin syndrome Generalized lichen myxedematosus Secondary mucinoses Basal-cell carcinoma Granuloma annulare
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Cinchonism
Wikipedia
Classification D ICD - 10 : T37.2 ICD - 9-CM : 386.9 , 961.4 DiseasesDB : 11124 v t e Diseases of the outer and middle ear Outer ear Otitis externa Otomycosis Middle ear and mastoid Otitis media Mastoiditis Bezold's abscess Gradenigo's syndrome Tympanosclerosis Cholesteatoma Perforated eardrum Symptoms Ear pain Hearing loss Tests Otoscope pneumatic tympanometry v t e Poisoning Toxicity Overdose History of poison Inorganic Metals Toxic metals Beryllium Cadmium Lead Mercury Nickel Silver Thallium Tin Dietary minerals Chromium Cobalt Copper Iron Manganese Zinc Metalloids Arsenic Nonmetals Sulfuric acid Selenium Chlorine Fluoride Organic Phosphorus Pesticides Aluminium phosphide Organophosphates Nitrogen Cyanide Nicotine Nitrogen dioxide poisoning CHO alcohol Ethanol Ethylene glycol Methanol Carbon monoxide Oxygen Toluene Pharmaceutical Drug overdoses Nervous Anticholinesterase Aspirin Barbiturates Benzodiazepines Cocaine Lithium Opioids Paracetamol Tricyclic antidepressants Cardiovascular Digoxin Dipyridamole Vitamin poisoning Vitamin A Vitamin D Vitamin E Megavitamin-B 6 syndrome Biological 1 Fish / seafood Ciguatera Haff disease Ichthyoallyeinotoxism Scombroid Shellfish poisoning Amnesic Diarrhetic Neurotoxic Paralytic Other vertebrates amphibian venom Batrachotoxin Bombesin Bufotenin Physalaemin birds / quail Coturnism snake venom Alpha-Bungarotoxin Ancrod Batroxobin Arthropods Arthropod bites and stings bee sting / bee venom Apamin Melittin scorpion venom Charybdotoxin spider venom Latrotoxin / Latrodectism Loxoscelism tick paralysis Plants / fungi Cinchonism Ergotism Lathyrism Locoism Mushrooms Strychnine 1 including venoms , toxins , foodborne illnesses .
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Haemolacria
Wikipedia
It was suggested that she could have had an unknown disease, but more skeptical views hypothesized that the case might be explained by Münchausen syndrome by proxy , where her mother, seemingly the only one to witness her bleeding actually starting, was fabricating the story and somehow inducing the effect on the girl. [6] Sanal Edamaruku observed in 2010 that the pattern seemed to match her menstrual cycle and believed that she was faking the symptoms. [7] Calvino Inman Aged 22, reported to weep tears of blood 5 times a day. [8] Rashida Khatoon From India, was reportedly crying blood up to five times a day in 2009, and fainting with every weeping. [9] Débora Santos Age 17, from Brazil. ... She was diagnosed after 2008 with Gardner–Diamond syndrome for her random bruising, but in 2010 had symptoms of the splitting of her tongue which would bleed profusely.
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Spermatocele
Wikipedia
External links [ edit ] Classification D ICD - 10 : N43.4 ICD - 9-CM : 608.1 MeSH : D013088 DiseasesDB : 31243 SNOMED CT : 49263001 v t e Male diseases of the pelvis and genitals Internal Testicular Orchitis Hydrocele testis Testicular cancer Testicular torsion Male infertility Aspermia Asthenozoospermia Azoospermia Hyperspermia Hypospermia Oligospermia Necrospermia Teratospermia Epididymis Epididymitis Spermatocele Hematocele Prostate Prostatitis Acute prostatitis Chronic bacterial prostatitis Chronic prostatitis/chronic pelvic pain syndrome Asymptomatic inflammatory prostatitis Benign prostatic hyperplasia Prostate cancer Seminal vesicle Seminal vesiculitis External Penis Balanoposthitis / Balanitis Balanitis plasmacellularis Pseudoepitheliomatous keratotic and micaceous balanitis Phimosis Paraphimosis Priapism Sexual dysfunction Erectile dysfunction Peyronie's disease Penile cancer Penile fracture Balanitis xerotica obliterans Other Hematospermia Retrograde ejaculation Postorgasmic illness syndrome
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Lipoatrophia Semicircularis
Wikipedia
External links [ edit ] Classification D ICD - 10 : L90.8 ( ILDS L90.876) v t e Cutaneous keratosis, ulcer, atrophy, and necrobiosis Epidermal thickening keratoderma : Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis : Seborrheic keratosis Clonal seborrheic keratosis Common seborrheic keratosis Irritated seborrheic keratosis Seborrheic keratosis with squamous atypia Reticulated seborrheic keratosis Dermatosis papulosa nigra Keratosis punctata of the palmar creases other hyperkeratosis : Acanthosis nigricans Confluent and reticulated papillomatosis Callus Ichthyosis acquisita Arsenical keratosis Chronic scar keratosis Hyperkeratosis lenticularis perstans Hydrocarbon keratosis Hyperkeratosis of the nipple and areola Inverted follicular keratosis Lichenoid keratosis Multiple minute digitate hyperkeratosis PUVA keratosis Reactional keratosis Stucco keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: Keloid Hypertrophic scar Cutis verticis gyrata Necrobiosis / granuloma Necrobiotic/palisading Granuloma annulare Perforating Generalized Subcutaneous Granuloma annulare in HIV disease Localized granuloma annulare Patch-type granuloma annulare Necrobiosis lipoidica Annular elastolytic giant-cell granuloma Granuloma multiforme Necrobiotic xanthogranuloma Palisaded neutrophilic and granulomatous dermatitis Rheumatoid nodulosis Interstitial granulomatous dermatitis / Interstitial granulomatous drug reaction Foreign body granuloma Beryllium granuloma Mercury granuloma Silica granuloma Silicone granuloma Zirconium granuloma Soot tattoo Tattoo Carbon stain Other/ungrouped eosinophilic dermatosis Granuloma faciale Dermis / localized CTD Cutaneous lupus erythematosus chronic: Discoid Panniculitis subacute : Neonatal ungrouped: Chilblain Lupus erythematosus–lichen planus overlap syndrome Tumid Verrucous Rowell's syndrome Scleroderma / Morphea Localized scleroderma Localized morphea Morphea–lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma Atrophic / atrophoderma Lichen sclerosus Anetoderma Schweninger–Buzzi anetoderma Jadassohn–Pellizzari anetoderma Atrophoderma of Pasini and Pierini Acrodermatitis chronica atrophicans Semicircular lipoatrophy Follicular atrophoderma Linear atrophoderma of Moulin Perforating Kyrle disease Reactive perforating collagenosis Elastosis perforans serpiginosa Perforating folliculitis Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum / Pseudo-ainhum This cutaneous condition article is a stub .
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Pretibial Myxedema
Wikipedia
External links [ edit ] Classification D ICD - 9-CM : 242.9 DiseasesDB : 25147 External resources eMedicine : derm/347 v t e Thyroid disease Hypothyroidism Iodine deficiency Cretinism Congenital hypothyroidism Myxedema Myxedema coma Euthyroid sick syndrome Signs and symptoms Queen Anne's sign Woltman sign Thyroid dyshormonogenesis Pickardt syndrome Hyperthyroidism Hyperthyroxinemia Thyroid hormone resistance Familial dysalbuminemic hyperthyroxinemia Hashitoxicosis Thyrotoxicosis factitia Thyroid storm Graves' disease Signs and symptoms Abadie's sign of exophthalmic goiter Boston's sign Dalrymple's sign Stellwag's sign lid lag Griffith's sign Möbius sign Pretibial myxedema Graves' ophthalmopathy Thyroiditis Acute infectious Subacute De Quervain's Subacute lymphocytic Palpation Autoimmune /chronic Hashimoto's Postpartum Riedel's Enlargement Goitre Endemic goitre Toxic nodular goitre Toxic multinodular goiter Thyroid nodule Colloid nodule
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Urinary Bladder Disease
Wikipedia
Cystitis is common, sometimes referred to as urinary tract infection (UTI) caused by bacteria, bladder rupture occurs when the bladder is overfilled and not emptied while bladder tamponade is a result of blood clot formation near the bladder outlet. [1] Contents 1 Cystitis 2 Bladder trauma 2.1 Intra- and extraperitoneal rupture 3 Bladder tamponade 4 See also 5 References 6 External links Cystitis [ edit ] Main article: Cystitis Cystitis is a urinary bladder inflammation that results from any one of a number of distinct syndromes. [2] It is most commonly caused by a bacterial infection in which case it is referred to as a urinary tract infection. [3] Bladder trauma [ edit ] Bladder rupture (rupture of bladder, N32.4 ) may occur if the bladder is overfilled and not emptied. ... External links [ edit ] Classification D ICD - 10 : N30 - N33 , Q64.0 - Q64.1 ICD - 9-CM : 595 - 596 , 752.61 - 752.62 MeSH : D001745 Wikimedia Commons has media related to Diseases and disorders of the human urinary bladder . http://kidney.niddk.nih.gov/kudiseases/topics/bladder.asp v t e Diseases of the urinary tract Ureter Ureteritis Ureterocele Megaureter Bladder Cystitis Interstitial cystitis Hunner's ulcer Trigonitis Hemorrhagic cystitis Neurogenic bladder dysfunction Bladder sphincter dyssynergia Vesicointestinal fistula Vesicoureteral reflux Urethra Urethritis Non-gonococcal urethritis Urethral syndrome Urethral stricture Meatal stenosis Urethral caruncle Any/all Obstructive uropathy Urinary tract infection Retroperitoneal fibrosis Urolithiasis Bladder stone Kidney stone Renal colic Malakoplakia Urinary incontinence Stress Urge Overflow
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Uterine Malformation
Wikipedia
The condition is also called Mayer-Rokitansky-Kuster-Hauser syndrome. The patient with MRKH syndrome will have primary amenorrhea .
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Intraocular Lymphoma
Wikipedia
What is more, while the vast majority of PCNSL in patients with acquired immune deficiency syndrome (AIDS) is related to the Epstein-Barr virus (EBV), the development of PCNSL and PIOL in immunocompetent patients is unknown and shows no general relation to infectious DNAs. [1] In immunocompetent patients, PIOL most commonly affects patients in their fifties and sixties. ... Fluorescein angiography may reveal "leopard spot" patterns due to sub-RPE infiltrates that stain early and progressively or mottling of the RPE due to hyper- and hypofluorescent window defects. [2] PIOL is known as a masquerade syndrome because it frequently simulates the signs and symptoms of uveitis.
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Anosodiaphoria
Wikipedia
It is a somatosensory agnosia , or a sign of neglect syndrome . [1] It might be specifically associated with defective functioning of the frontal lobe of the right hemisphere. [2] Joseph Babinski first used the term anosodiaphoria in 1914 to describe a disorder of the body schema in which patients verbally acknowledge a clinical problem (such as hemiparesis ) but fail to be concerned about it. [3] Anosodiaphoria follows a stage of anosognosia , in which there may be verbal, explicit denial of the illness, and after several days to weeks, develop the lack of emotional response. [4] Indifference is different from denial because it implies a lack of caring on the part of the patient, who otherwise acknowledges his or her deficit. ... These emotional disorders cannot account for the verbal explicit denial of illness of anosognosia . [5] Other explanations include reduced emotional experience, impaired emotional communication, alexithymia , behavioral abnormalities , dysexecutive syndrome , and the frontal lobes . [6] Neurology [ edit ] Anosodiaphoria occurs after stroke of the brain. 27% of patients suffering from an acute hemispheric stroke suffer the stroke in the right hemisphere, while 2% suffer it in their left. [7] Anosodiaphoria is thought to be related to unilateral neglect , a condition often found after damage to the non-dominant (usually the right) hemisphere of the cerebral cortex in which sufferers seem unable to attend to, or sometimes comprehend, anything on a certain side of their body (usually the left).
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Pulmonary Interstitial Emphysema
Wikipedia
Contents 1 Cause 2 Pathophysiology 3 Diagnosis 4 Treatment 5 Prognosis 6 Epidemiology 6.1 United States 6.2 International 7 See also 8 References 9 External links Cause [ edit ] Pulmonary interstitial emphysema is a concern in any of the following: Prematurity Infant respiratory distress syndrome (IRDS) Meconium aspiration syndrome (MAS) Amniotic fluid aspiration Sepsis Infections Mechanical ventilation Pathophysiology [ edit ] Pulmonary interstitial emphysema is created when air bursts or ruptures through tissue from the alveoli and bronchioles into the perivascular tissue of the lung.
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Mental Retardation, Autosomal Dominant 41
Omim
Electroencephalogram (EEG) later showed hypsarrhythmia and brain MRI revealed no structural brain anomalies; these features were consistent with a clinical diagnosis of West syndrome. She had no eye fixation or pursuit at age 7 months and had mild dysmorphic features. ... One radiograph available from childhood showed cone-shaped epiphysis of the proximal phalanx of the right great toe. The patient also had Tourette syndrome (137580), which was also present in his otherwise unaffected brother.
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Nodular Sclerosis
Wikipedia
External links [ edit ] PubMed - use of Erythropoietin Subtypes Lymphoma Association information on nodular sclerosing Classification D ICD - 10 : C81.1 ICD - 9-CM : 201.5 ICD-O : M9663/3 -9667/3 v t e Leukaemias , lymphomas and related disease B cell ( lymphoma , leukemia ) (most CD19 CD20 ) By development/ marker TdT+ ALL ( Precursor B acute lymphoblastic leukemia/lymphoma ) CD5 + naive B cell ( CLL/SLL ) mantle zone ( Mantle cell ) CD22 + Prolymphocytic CD11c+ ( Hairy cell leukemia ) CD79a + germinal center / follicular B cell ( Follicular Burkitt's GCB DLBCL Primary cutaneous follicle center lymphoma ) marginal zone / marginal zone B-cell ( Splenic marginal zone MALT Nodal marginal zone Primary cutaneous marginal zone lymphoma ) RS ( CD15 +, CD30 +) Classic Hodgkin lymphoma ( Nodular sclerosis ) CD20+ ( Nodular lymphocyte predominant Hodgkin lymphoma ) PCDs / PP ( CD38 +/ CD138 +) see immunoproliferative immunoglobulin disorders By infection KSHV ( Primary effusion ) EBV Lymphomatoid granulomatosis Post-transplant lymphoproliferative disorder Classic Hodgkin lymphoma Burkitt's lymphoma HCV Splenic marginal zone lymphoma HIV ( AIDS-related lymphoma ) Helicobacter pylori ( MALT lymphoma ) Cutaneous Diffuse large B-cell lymphoma Intravascular large B-cell lymphoma Primary cutaneous marginal zone lymphoma Primary cutaneous immunocytoma Plasmacytoma Plasmacytosis Primary cutaneous follicle center lymphoma T/NK T cell ( lymphoma , leukemia ) (most CD3 CD4 CD8 ) By development/ marker TdT+ : ALL ( Precursor T acute lymphoblastic leukemia/lymphoma ) prolymphocyte ( Prolymphocytic ) CD30+ ( Anaplastic large-cell lymphoma Lymphomatoid papulosis type A ) Cutaneous MF+variants indolent: Mycosis fungoides Pagetoid reticulosis Granulomatous slack skin aggressive: Sézary disease Adult T-cell leukemia/lymphoma Non-MF CD30 -: Non-mycosis fungoides CD30− cutaneous large T-cell lymphoma Pleomorphic T-cell lymphoma Lymphomatoid papulosis type B CD30 +: CD30+ cutaneous T-cell lymphoma Secondary cutaneous CD30+ large-cell lymphoma Lymphomatoid papulosis type A Other peripheral Hepatosplenic Angioimmunoblastic Enteropathy-associated T-cell lymphoma Peripheral T-cell lymphoma not otherwise specified ( Lennert lymphoma ) Subcutaneous T-cell lymphoma By infection HTLV-1 ( Adult T-cell leukemia/lymphoma ) NK cell / (most CD56 ) Aggressive NK-cell leukemia Blastic NK cell lymphoma T or NK EBV ( Extranodal NK-T-cell lymphoma / Angiocentric lymphoma ) Large granular lymphocytic leukemia Lymphoid+ myeloid Acute biphenotypic leukaemia Lymphocytosis Lymphoproliferative disorders ( X-linked lymphoproliferative disease Autoimmune lymphoproliferative syndrome ) Leukemoid reaction Diffuse infiltrative lymphocytosis syndrome Cutaneous lymphoid hyperplasia Cutaneous lymphoid hyperplasia with bandlike and perivascular patterns with nodular pattern Jessner lymphocytic infiltrate of the skin General Hematological malignancy leukemia Lymphoproliferative disorders Lymphoid leukemias This article about a neoplasm is a stub .KLHDC8B, HLA-DRB1, GJB2, LPP, CLEC16A, AHI1, UPF3A, HLA-DRB9, GATA3, SLC26A4, GJB6, PDLIM7, GJB3, RNR1, KRT20, IGH, TMC1, TNFRSF8, MS4A1, CCL17, CXCL9, MLC1, KCNQ4, ARHGAP44, CDC14A, TGFB1, NINL, BIRC5, DDX58, CD274, GPSM2, SPARC, TBC1D24, MIB1, TMPRSS3, GIPC3, RBM45, MIR127, TRBV20OR9-2, PLS1, SDC1, CCL22, BCL2, CCN2, CTSK, GSDME, DFNB13, DSPP, ELF3, ESRRB, HLA-DPB1, IFNG, IL13, IL13RA2, CXCL10, JAK1, JAK2, MITF, ABCC1, TRNS1, MYO6, ATM, REL, RNASE3, CCL11, MIR889
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Urogenital Neoplasm
Wikipedia
External links [ edit ] Classification D ICD - 10 : C50 - C68 D24 - D30.9 MeSH : D014565 v t e Overview of tumors , cancer and oncology Conditions Benign tumors Hyperplasia Cyst Pseudocyst Hamartoma Malignant progression Dysplasia Carcinoma in situ Cancer Metastasis Primary tumor Sentinel lymph node Topography Head and neck ( oral , nasopharyngeal ) Digestive system Respiratory system Bone Skin Blood Urogenital Nervous system Endocrine system Histology Carcinoma Sarcoma Blastoma Papilloma Adenoma Other Precancerous condition Paraneoplastic syndrome Staging / grading TNM Ann Arbor Prostate cancer staging Gleason grading system Dukes classification Carcinogenesis Cancer cell Carcinogen Tumor suppressor genes / oncogenes Clonally transmissible cancer Oncovirus Carcinogenic bacteria Misc. Research Index of oncology articles History Cancer pain Cancer and nausea v t e Tumors of the female urogenital system Adnexa Ovaries Glandular and epithelial / surface epithelial- stromal tumor CMS: Ovarian serous cystadenoma Mucinous cystadenoma Cystadenocarcinoma Papillary serous cystadenocarcinoma Krukenberg tumor Endometrioid tumor Clear-cell ovarian carcinoma Brenner tumour Sex cord–gonadal stromal Leydig cell tumour Sertoli cell tumour Sertoli–Leydig cell tumour Thecoma Granulosa cell tumour Luteoma Sex cord tumour with annular tubules Germ cell Dysgerminoma Nongerminomatous Embryonal carcinoma Endodermal sinus tumor Gonadoblastoma Teratoma / Struma ovarii Choriocarcinoma Fibroma Meigs' syndrome Fallopian tube Adenomatoid tumor Uterus Myometrium Uterine fibroids/leiomyoma Leiomyosarcoma Adenomyoma Endometrium Endometrioid tumor Uterine papillary serous carcinoma Endometrial intraepithelial neoplasia Uterine clear-cell carcinoma Cervix Cervical intraepithelial neoplasia Clear-cell carcinoma SCC Glassy cell carcinoma Villoglandular adenocarcinoma Placenta Choriocarcinoma Gestational trophoblastic disease General Uterine sarcoma Mixed Müllerian tumor Vagina Squamous-cell carcinoma of the vagina Botryoid rhabdomyosarcoma Clear-cell adenocarcinoma of the vagina Vaginal intraepithelial neoplasia Vaginal cysts Vulva SCC Melanoma Papillary hidradenoma Extramammary Paget's disease Vulvar intraepithelial neoplasia Bartholin gland carcinoma v t e Tumors of the male urogenital system Testicles Sex cord– gonadal stromal Sertoli–Leydig cell tumour Sertoli cell tumour Leydig cell tumour Germ cell G Seminoma Spermatocytic tumor Germ cell neoplasia in situ NG Embryonal carcinoma Endodermal sinus tumor Gonadoblastoma Teratoma Choriocarcinoma Embryoma Prostate Adenocarcinoma High-grade prostatic intraepithelial neoplasia HGPIN Small-cell carcinoma Transitional cell carcinoma Penis Carcinoma Extramammary Paget's disease Bowen's disease Bowenoid papulosis Erythroplasia of Queyrat Hirsuties coronae glandis v t e Tumors of the urinary and genital systems Kidney Glandular and epithelial neoplasm Renal cell carcinoma Renal oncocytoma Mixed tumor Wilms' tumor Mesoblastic nephroma Clear-cell sarcoma of the kidney Angiomyolipoma Cystic nephroma Metanephric adenoma by location Renal medullary carcinoma Juxtaglomerular cell tumor Renal medullary fibroma Ureter Ureteral neoplasm Bladder Transitional cell carcinoma Squamous-cell carcinoma Inverted papilloma Urethra Transitional cell carcinoma Squamous-cell carcinoma Adenocarcinoma Melanoma Other Malignant fibrous histiocytoma This women's health related article is a stub .
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Pagophagia
Wikipedia
PMID 2096423 . v t e Symptoms and signs relating to the human digestive system or abdomen Gastrointestinal tract Nausea Vomiting Heartburn Aerophagia Pagophagia Dysphagia oropharyngeal esophageal Odynophagia Bad breath Xerostomia Hypersalivation Burping Wet burp Goodsall's rule Chilaiditi syndrome Dance's sign Aaron's sign Arapov's sign Markle sign McBurney's point Sherren's triangle Radiologic signs : Hampton's line Klemm's sign Accessory liver : Councilman body Mallory body biliary: Boas' sign Courvoisier's law Charcot's cholangitis triad / Reynolds' pentad cholecystitis ( Murphy's sign Lépine's sign Mirizzi's syndrome ) Nardi test Defecation Flatulence Fecal incontinence Encopresis Fecal occult blood Rectal tenesmus Constipation Obstructed defecation Diarrhea Rectal discharge Psoas sign Obturator sign Rovsing's sign Hamburger sign Heel tap sign Aure-Rozanova's sign Dunphy sign Alder's sign Lockwood's sign Rosenstein's sign Abdomen Pain Abdominal pain Acute abdomen Colic Baby colic Abdominal guarding Blumberg sign Distension Abdominal distension Bloating Ascites Tympanites Shifting dullness Ascites Fluid wave test Masses Abdominal mass Hepatosplenomegaly Hepatomegaly Splenomegaly Other Jaundice Mallet-Guy sign Puddle sign Ballance's sign Aortic insufficiency Castell's sign Kehr's sign Cullen's sign Grey Turner's sign Hernia Howship–Romberg sign Hannington-Kiff sign Other Cupola sign Fothergill's sign Carnett's sign Sister Mary Joseph nodule
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Reticular Dysgenesis
Omim
Pannicke et al. (2009) stated that reticular dysgenesis is the first example of a human immunodeficiency syndrome that is causally linked to energy metabolism and that can therefore be classified as a mitochondriopathy. ... Lagresle-Peyrou et al. (2009) concluded that their results identified a previously unknown mechanism involved in regulation of hematopoietic cell differentiation in one of the most severe human immunodeficiency syndromes. INHERITANCE - Autosomal recessive HEMATOLOGY - Congenital agranulocytosis - Leukopenia - Lymphopenia - Absent bone marrow myeloid elements IMMUNOLOGY - Lymphoid hypoplasia - Thymic hypoplasia - Absent cellular immunity - Absent humoral immunity MISCELLANEOUS - Early death in the first few weeks of life MOLECULAR BASIS - Caused by mutation in the adenylate kinase-2 gene (AK2, 103020.0001 ) ▲ Close
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Telangiectasia, Hereditary Hemorrhagic, Type 5
Omim
Description Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant syndrome characterized by telangiectases and arteriovenous malformations (AVMs). ... However, hepatic MRI in this patient, who had abnormal liver enzymes and portal hypertension and had also been diagnosed with hepatopulmonary syndrome, showed vascular findings similar to those seen in HHT, with a slightly heterogeneous arterial phase and prominent, slightly corkscrew smaller branches of the hepatic artery as well as a suggestion of small focal nodular hyperplasia.
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Lipoyltransferase 1 Deficiency
Omim
The findings were consistent with a clinical diagnosis of Leigh syndrome (256000). Laboratory studies showed increased glutamine and proline and were consistent with decreased activities of the pyruvate dehydrogenase complex (PDHC) and alpha-ketoglutarate dehydrogenase (KGDH), as demonstrated in patient fibroblasts. ... INHERITANCE - Autosomal recessive CARDIOVASCULAR Heart - Bradycardia (patient B) Vascular - Pulmonary hypertension (patient B) ABDOMEN Liver - Liver dysfunction NEUROLOGIC Central Nervous System - Delayed psychomotor development (patient A) - j Hypertonia - Dystonic movements - Truncal hypotonia (patient A) - Spastic tetraparesis (patient A) - Extrapyramidal symptoms (patient A) - Cerebellar atrophy (patient A) - Thalamic abnormalities (patient A) - White matter abnormalities (patient A) - Delayed myelination (patient A) - Leigh syndrome (patient A) METABOLIC FEATURES - Lactic acidosis LABORATORY ABNORMALITIES - Abnormal liver enzymes - Increased bilirubin (patient B) - Increased serum alpha-ketoglutarate - Increased serum lactate - Increased serum alpha-alanine (patient B) - Increased serum glutamine (patient A) - Increased serum proline - Normal serum glycine - Absence of protein-bound lipoic acid - Decreased activity of branched-chain ketoacid dehydrogenase (BCKDH) - Decreased activity of alpha-ketoglutarate dehydrogenase (alpha-KGDH) - Decreased activity of pyruvate dehydrogenase complex (PDH) MISCELLANEOUS - Onset in infancy - Symptoms present as acute metabolic and clinical decompensation associated with infection - Death in infancy (patient B) - Two unrelated patients have been reported (last curated April 2015) MOLECULAR BASIS - Caused by mutation in the lipoyltransferase 1 gene (LIPT1, 610284.0001 ) ▲ Close
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Orthostatic Hypotensive Disorder, Streeten Type
Omim
It occurs also in amyloid polyneuropathy due to mutations in the TTR gene (176300), in the neuropathy of Fabry disease (301500), in deficiency of dopamine beta-hydroxylase (223360), and as a striking feature of familial dysautonomia (DYS; 223900). Shy-Drager syndrome (146500) is a disorder of progressive autonomic failure with orthostatic hypotension as a leading feature. The syndrome is probably genetically heterogeneous.