Lymphoma, and Hypotension

Diseases related with Lymphoma and Hypotension

In the following list you will find some of the most common rare diseases related to Lymphoma and Hypotension that can help you solving undiagnosed cases.

Top matches:

The Heidelberg histologic classification of renal cell tumors subdivides renal cell tumors into benign and malignant parenchymal neoplasms and, where possible, limits each subcategory to the most common documented genetic abnormalities (Kovacs et al., 1997). Malignant tumors are subclassified into common or conventional renal cell carcinoma (clear cell); papillary renal cell carcinoma; chromophobe renal cell carcinoma; collecting duct carcinoma, with medullary carcinoma of the kidney; and unclassified renal cell carcinoma. The common or conventional type accounts for about 75% of renal cell neoplasms and is characterized genetically by a highly specific deletion of chromosome 3p. Papillary renal cell carcinoma (see {605074}) accounts for about 10% of renal cell tumors. Chromophobe renal cell carcinoma accounts for approximately 5% of renal cell neoplasms. Genetically, chromophobe RCC is characterized by a combination of loss of heterozygosity of chromosomes 1, 2, 6, 10, 13, 17, and 21 and hypodiploid DNA content. Collecting duct carcinoma accounts for about 1% of renal cell carcinoma.Renal cell carcinoma occurs nearly twice as often in men as in women; incidence in the United States is equivalent among whites and blacks. Cigarette smoking doubles the likelihood of renal cell carcinoma and contributes to as many as one-third of cases. Obesity is also a risk factor, particularly in women. Other risk factors include hypertension, unopposed estrogen therapy, and occupational exposure to petroleum products, heavy metals, or asbestos (summary by Motzer et al., 1996). Genetic Heterogeneity of Renal Cell CarcinomaGermline mutation resulting in nonpapillary renal cell carcinoma of the clear cell and chromophobe type occurs in the HNF1A gene (OMIM ) and the HNF1B gene (OMIM ).Somatic mutations in renal cell carcinomas occur in the VHL gene (OMIM ), the TRC8 gene (OMIM ), the OGG1 gene (OMIM ), the ARMET gene (OMIM ), the FLCN gene (OMIM ), and the BAP1 gene (OMIM ).See also RCCX1 (OMIM ) for a discussion of renal cell carcinoma associated with translocations of chromosome Xp11.2 involving the TFE3 gene (OMIM ).For a discussion of papillary renal cell carcinoma, see RCCP1 (OMIM ). Occurrence of Renal Cell Carcinoma in Other DisordersVon Hippel-Lindau syndrome (OMIM ) is a familial multicancer syndrome in which there is a susceptibility to a variety of neoplasms, including renal cell carcinoma of clear cell histology and renal cysts. A syndrome of predisposition to uterine leiomyomas and papillary renal cell carcinoma has been reported (OMIM ). Medullary carcinoma of the kidney is believed to arise from the collecting ducts of the renal medulla and is associated with sickle cell trait (OMIM ) (Kovacs et al., 1997). Renal cell carcinoma occurs in patients with the Birt-Hogg-Dube syndrome (OMIM ).Bertolotto et al. (2011) identified a missense mutation in the MITF (OMIM ) gene that increases the risk of renal cell carcinoma with or without malignant melanoma (CMM8 ).

RENAL CELL CARCINOMA, NONPAPILLARY; RCC Is also known as hypernephroma|adenocarcinoma of kidney

Related symptoms:

  • Neoplasm
  • Hypertension
  • Obesity
  • Carcinoma
  • Falls


SOURCES: OMIM ORPHANET MENDELIAN

More info about RENAL CELL CARCINOMA, NONPAPILLARY; RCC

Essential thrombocythemia (ET) is a myeloproliferative neoplasm (MPN, see this term) characterized by a sustained elevation of platelet number (> 450 x 109/L) with a tendency for thrombosis and hemorrhage.

ESSENTIAL THROMBOCYTHEMIA Is also known as thrombocytosis 1|essential thrombocytosis|et

Related symptoms:

  • Pain
  • Hypertension
  • Hepatomegaly
  • Abnormality of the skeletal system
  • Respiratory distress


SOURCES: ORPHANET OMIM MENDELIAN

More info about ESSENTIAL THROMBOCYTHEMIA

Low match KAPOSI SARCOMA

Kaposi sarcoma (KS) is a rare human herpes virus 8 (HHV-8)-induced endothelial inflammatory neoplasm that develops is various clinically distinct settings, manifesting mostly as cutaneous lesions, or mucosal or visceral involvement.

KAPOSI SARCOMA Is also known as multiple idiopathic pigmented hemangiosarcoma, susceptibility to

Related symptoms:

  • Neoplasm
  • Hypertension
  • Fever
  • Fatigue
  • Edema


SOURCES: OMIM ORPHANET MENDELIAN

More info about KAPOSI SARCOMA

Other less relevant matches:

Dyskeratosis congenita is an inherited bone marrow failure syndrome classically characterized by the triad of mucosal leukoplakia, nail dysplasia, and abnormal skin pigmentation. Affected individuals have an increased risk of aplastic anemia and malignancy. Less common features include epiphora, premature gray hair, microcephaly, developmental delay, and pulmonary fibrosis, among others. The phenotype is highly variable. All affected individuals have shortened telomeres due to a defect in telomere maintenance (summary by Savage et al., 2008).For a discussion of genetic heterogeneity of dyskeratosis congenita, see DCKA1 (OMIM ).

Related symptoms:

  • Global developmental delay
  • Short stature
  • Hearing impairment
  • Microcephaly
  • Ataxia


SOURCES: OMIM MENDELIAN

More info about DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3

Severe combined immunodeficiency (SCID) due to adenosine deaminase (ADA) deficiency is a form of SCID characterized by profound lymphopenia and very low immunoglobulin levels of all isotypes resulting in severe and recurrent opportunistic infections.

SEVERE COMBINED IMMUNODEFICIENCY DUE TO ADENOSINE DEAMINASE DEFICIENCY Is also known as ada deficiency|ada-scid|scid due to adenosine deaminase deficiency|scid due to ada deficiency|scid due to ada deficiency, early-onset

Related symptoms:

  • Global developmental delay
  • Failure to thrive
  • Hypertension
  • Hepatomegaly
  • Abnormality of the skeletal system


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about SEVERE COMBINED IMMUNODEFICIENCY DUE TO ADENOSINE DEAMINASE DEFICIENCY

Dopamine beta-hydroxylase deficiency is an extremely rare genetic metabolic disorder characterized by autonomic dysregulation leading mainly to orthostatic hypotension.

DOPAMINE BETA-HYDROXYLASE DEFICIENCY Is also known as norepinephrine deficiency|noradrenaline deficiency

Related symptoms:

  • Seizures
  • Generalized hypotonia
  • Muscular hypotonia
  • Pain
  • Ptosis


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about DOPAMINE BETA-HYDROXYLASE DEFICIENCY

Hereditary angioedema type 1 (HAE 1) is a form of hereditary angioedema (see this term) characterized by acute edema in subcutaneous tissues, viscera and/or the upper airway.

HEREDITARY ANGIOEDEMA TYPE 1 Is also known as hae 1|angioneurotic edema, hereditary|hereditary angioneurotic edema type 1|hae-i|hane|c1 esterase inhibitor, deficiency of

Related symptoms:

  • Pain
  • Peripheral neuropathy
  • Dysphagia
  • Respiratory distress
  • Edema


SOURCES: ORPHANET OMIM MENDELIAN

More info about HEREDITARY ANGIOEDEMA TYPE 1

Mastocytosis, or mast cell disease, is a heterogeneous group of clinical disorders characterized by the abnormal accumulation of mast cells in various tissues, especially in the skin and hematopoietic organs. Mastocytosis usually appears in infancy or early adulthood. In most pediatric cases, the disease is limited to the skin, but it can be associated with systemic symptoms due to the release of mediators from mast cells, even when there is no systemic infiltration. It usually has a good prognosis, with substantial improvement or spontaneous resolution before puberty. In rare cases, the disease may remain active through adolescence as a systemic adult mastocytosis. Cutaneous mastocytosis is characterized by macules, papules, nodules, or diffuse infiltration of the skin, often associated with localized hyperpigmentation. Gentle rubbing of the lesions induces histamine release from mechanically activated mast cells, causing local wheals, erythema, and often pruritus, a phenomenon termed the 'Darier sign.' In contrast to childhood-onset mastocytosis, adult-onset mastocytosis often persists for the lifetime of the patient and is also more likely to be a severe and systemic disease involving numerous organs. In some cases, it is associated with a clonal hematologic non-mast-cell lineage disease, such as a myelodysplastic or myeloproliferative disorder. Adult-onset mastocytosis can also lead to the rare mast cell leukemia, which carries a high risk of mortality (summary by Bodemer et al., 2010 and Kambe et al., 2010).

MASTOCYTOSIS, CUTANEOUS; MASTC Is also known as mastocytosis, maculopapular cutaneous|mastocytosis, diffuse cutaneous|urticaria pigmentosa

Related symptoms:

  • Neoplasm
  • Pain
  • Anemia
  • Hypertension
  • Hepatomegaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about MASTOCYTOSIS, CUTANEOUS; MASTC

Achondroplasia is the most frequent form of short-limb dwarfism. Affected individuals exhibit short stature caused by rhizomelic shortening of the limbs, characteristic facies with frontal bossing and midface hypoplasia, exaggerated lumbar lordosis, limitation of elbow extension, genu varum, and trident hand (summary by Bellus et al., 1995).

Related symptoms:

  • Intellectual disability
  • Short stature
  • Generalized hypotonia
  • Hearing impairment
  • Scoliosis


SOURCES: MESH OMIM MENDELIAN

More info about ACHONDROPLASIA; ACH

Familial amyloid polyneuropathy (FAP) or transthyretin (TTR) amyloid polyneuropathy is a progressive sensorimotor and autonomic neuropathy of adulthood onset. Weight loss and cardiac involvement are frequent; ocular or renal complications may also occur.

ATTRV30M AMYLOIDOSIS Is also known as familial amyloid polyneuropathy type i|ttr amyloid neuropathy|attrv30m-related amyloidosis|hereditary amyloidosis, transthyretin-related|transthyretin amyloid polyneuropathy|familial amyloid polyneuropathy, portuguese-swedish-japanese type|fap|amyloid pol

Related symptoms:

  • Seizures
  • Hearing impairment
  • Ataxia
  • Nystagmus
  • Sensorineural hearing impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about ATTRV30M AMYLOIDOSIS

Top 5 symptoms//phenotypes associated to Lymphoma and Hypotension

Symptoms // Phenotype % cases
Hypertension Common - Between 50% and 80% cases
Pain Common - Between 50% and 80% cases
Diarrhea Uncommon - Between 30% and 50% cases
Weight loss Uncommon - Between 30% and 50% cases
Neoplasm Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Lymphoma and Hypotension. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Leukemia Anemia Multiple myeloma Abnormal lung morphology Gastrointestinal hemorrhage Paresthesia Hepatosplenomegaly Headache Splenomegaly Abnormality of the skeletal system Hepatomegaly Peripheral neuropathy Vomiting Edema Hearing impairment

Rare Symptoms - Less than 30% cases

Immunodeficiency Pneumonia Seizures Amyloidosis Portal hypertension Osteoporosis Skin rash Papule Lymphadenopathy Fatigue Fever Leukopenia Abnormal autonomic nervous system physiology Orthostatic hypotension Cellular immunodeficiency Ataxia Myelopathy Short stature Global developmental delay Myalgia Abnormality of the nervous system Delayed speech and language development Sarcoma Lymphoproliferative disorder Generalized hypotonia Thrombocytopenia Growth delay Bone marrow hypocellularity Hypermelanotic macule Epiphora Hydrocephalus Vertigo Paraparesis Dermatographic urticaria Respiratory distress Dyspnea Asthma Abdominal pain Malnutrition Recurrent otitis media Allergy Upper airway obstruction Abnormality of pelvic girdle bone morphology Axonal degeneration Myeloid leukemia Arrhythmia Malabsorption Obesity Erythema Peripheral axonal neuropathy Myeloproliferative disorder Urticaria Nausea Vasculitis Arthralgia Acute leukemia Gastroesophageal reflux Autoimmunity Clonus Skeletal dysplasia Short toe Recurrent urinary tract infections Severe short stature Rhizomelia Rigidity Midface retrusion Abnormality of the metaphysis Hyperlordosis Joint hyperflexibility Scarring Confusion Oral cleft Sleep disturbance Otitis media Overgrowth Conductive hearing impairment Lumbar hyperlordosis Epidermal acanthosis Tetraparesis Osteoarthritis Apnea Cleft lip Abnormal form of the vertebral bodies Micromelia Scoliosis Malar flattening Bone pain Hypersplenism Generalized osteosclerosis Flushing Abnormality of blood and blood-forming tissues Loss of consciousness Shock Osteolysis Telangiectasia Immunologic hypersensitivity Abnormal blistering of the skin Sudden cardiac death Ascites Recurrent fractures Tachycardia Cirrhosis Ichthyosis Gastrointestinal stroma tumor Asthenia Ventriculomegaly Sleep apnea Frontal bossing Macrocephaly Brachydactyly Hyperreflexia Depressed nasal bridge Motor delay Flexion contracture Intellectual disability Impaired temperature sensation Telangiectasia macularis eruptiva perstans Chronic leukemia Anaphylactic shock Cutaneous mastocytosis Mastocytosis Abnormality of the gastric mucosa Food intolerance Abnormal eosinophil morphology Acanthosis nigricans Osteopetrosis Infantile muscular hypotonia Arthritis Neuronal loss in central nervous system Migraine Urinary incontinence Gliosis Coma Polyneuropathy Nephropathy Paraplegia Facial palsy Dementia Bilateral sensorineural hearing impairment Constipation Hyporeflexia Areflexia Renal insufficiency Congestive heart failure Cardiomyopathy Tremor Dysarthria Visual impairment Peripheral demyelination Cardiomegaly Muscle weakness Restrictive cardiomyopathy Cardiac amyloidosis Vitreous floaters Orthostatic hypotension due to autonomic dysfunction Psychomotor deterioration Urinary retention Sensory ataxia Abnormal renal physiology Constrictive median neuropathy Stroke-like episode Increased CSF protein Hemiparesis Syringomyelia Decreased number of peripheral myelinated nerve fibers Aphasia Impotence Cerebral hemorrhage Rheumatoid arthritis Cachexia Atrioventricular block Spastic paraparesis Hallucinations Spasticity Sensorineural hearing impairment Short long bone Tibial bowing Generalized joint laxity Megalencephaly Spinal cord compression Obstructive sleep apnea Abnormality of the elbow Spinal canal stenosis Hip contracture Neuroblastoma Disproportionate short stature Limited elbow extension Dysuria Bowel incontinence Short femoral neck Flared metaphysis Spondyloepiphyseal dysplasia Chronic otitis media Epiphyseal dysplasia Back pain Genu varum Tinnitus Disproportionate short-limb short stature Communicating hydrocephalus Central apnea Nystagmus Cervical cord compression Lumbar kyphosis in infancy Myelitis Spinal stenosis with reduced interpedicular distance Trident hand Limited hip extension Brain stem compression Childhood onset short-limb short stature Small foramen magnum Iritis Hypopnea Abnormality of femur morphology Obstructive lung disease Cervical myelopathy Central sleep apnea Neonatal short-limb short stature Chronic myelogenous leukemia Thoracolumbar kyphosis Recurrent ear infections Hypoxemia Multiple epiphyseal dysplasia Cor pulmonale Nausea and vomiting Dysphagia Pruritus Venous insufficiency Intrauterine growth retardation Cryptorchidism Microcephaly Neoplasm by anatomical site Susceptibility to herpesvirus Skin plaque Generalized lymphadenopathy Skin nodule Cerebellar hypoplasia Abnormality of the spleen Abnormality of the lower limb Abnormality of the gastrointestinal tract Macule Abnormal retinal morphology Hemangioma Neoplasm of the skin Lymphedema Alopecia Osteopenia Abnormality of the liver Pulmonary fibrosis Esophageal stricture Aplastic anemia Oral leukoplakia Aseptic necrosis Hodgkin lymphoma Interstitial pulmonary abnormality Premature graying of hair Abnormal intestine morphology Retinopathy Hyperpigmentation of the skin Fine hair Pancytopenia Cerebral calcification Nail dysplasia Abnormality of skin pigmentation Dry skin Nail dystrophy Pulmonary arterial hypertension Encephalopathy Reticulated skin pigmentation Papillary renal cell carcinoma Bruising susceptibility Hemangioblastoma Cerebellar hemangioblastoma Small cell lung carcinoma Clear cell renal cell carcinoma Burkitt lymphoma Fibrosarcoma Retinoblastoma Myocardial infarction Renal neoplasm Renal cell carcinoma Polycythemia Nephroblastoma Melanoma Renal cyst Falls Carcinoma Chest pain Venous thrombosis Increased megakaryocyte count Abnormal thrombocyte morphology Abnormal platelet aggregation Decreased mean platelet volume Abnormal platelet morphology Bloody diarrhea Myelofibrosis Abnormality of bone marrow cell morphology Amaurosis fugax Impaired platelet aggregation Arterial thrombosis Myelodysplasia Abnormality of the cerebral vasculature Gangrene Acrocyanosis Transient ischemic attack Thrombocytosis Pulmonary embolism Prolonged bleeding time Leukocytosis Phimosis Pulmonary hemorrhage Abnormality of salivation Blurred vision Abnormality of metabolism/homeostasis Retrograde ejaculation Intermittent hypothermia Nocturia Recurrent hypoglycemia Hypothermia Neonatal hypoglycemia Dehydration Polycystic ovaries Syncope Hypoglycemia High palate Ptosis Muscular hypotonia Absent specific antibody response Reduced red cell adenosine deaminase activity Anti-thyroid peroxidase antibody positivity Hoarse voice Systemic lupus erythematosus Severe B lymphocytopenia Abnormal soft palate morphology Limbal edema Laryngeal edema Abnormal epiglottis morphology Tongue edema Abnormality of the uvula Intestinal edema Pharyngeal edema Abnormal respiratory system morphology Cryoglobulinemia Glomerulonephritis Edema of the dorsum of hands Facial edema Angioedema Inspiratory stridor Chronic lymphatic leukemia Ovarian cyst Abnormality of the larynx Stridor Lack of T cell function Abnormality of humoral immunity Failure to thrive Sinusitis Recurrent upper respiratory tract infections Eosinophilia Leukoencephalopathy Purpura Recurrent bacterial infections Recurrent pneumonia Lymphopenia Chronic diarrhea Autoimmune hemolytic anemia Inflammatory abnormality of the skin Hepatitis Sepsis Neutropenia Platyspondyly Respiratory tract infection Recurrent respiratory infections Recurrent infections Combined immunodeficiency IgA deficiency Absent tonsils B lymphocytopenia Absence of lymph node germinal center Immunoglobulin IgG2 deficiency Recurrent opportunistic infections Cortical sclerosis Aplasia of the thymus Anterior rib cupping Recurrent fungal infections Diffuse mesangial sclerosis Decrease in T cell count Autoimmune thrombocytopenia Pulmonary insufficiency Increased IgE level IgM deficiency Verrucae Recurrent viral infections B-cell lymphoma Recurrent lower respiratory tract infections Severe combined immunodeficiency Amyloid deposition in the vitreous humor


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