Edema, and Neoplasm of the skin
Diseases related with Edema and Neoplasm of the skin
In the following list you will find some of the most common rare diseases related to Edema and Neoplasm of the skin that can help you solving undiagnosed cases.
Low match BURULI ULCER, SUSCEPTIBILITY TO
Buruli ulcer is an infectious disease prevalent in many tropical and subtropical regions caused by infection with Mycobacterium ulcerans. It is the third most frequent mycobacterial disease in humans worldwide, after tuberculosis (OMIM ) and leprosy (OMIM ). Lesions are most common on exposed parts of the body, especially the limbs. Buruli ulcer derives its name from a county in Uganda, East Africa, north of Kampala, where the disease was found in the late 1950s in hundreds of people living near marshes and riverine areas near the Nile River (Clancey et al., 1961; Barker, 1971). The disease was first described in the medical literature in 1948 in a report on patients in Australia (MacCallum et al., 1948). Patients have also been reported from tropical areas in Latin America and Asia (Stienstra et al., 2006; van der Werf et al., 2005).
BURULI ULCER, SUSCEPTIBILITY TO Is also known as mycobacterium ulcerans, susceptibility toRelated symptoms:
More info about BURULI ULCER, SUSCEPTIBILITY TO
Low match UV-SENSITIVE SYNDROME 3; UVSS3
UV-sensitive syndrome-3 is an autosomal recessive disorder characterized by cutaneous photosensitivity and slight dyspigmentation, without an increased risk of skin tumors. Patient cells show impaired recovery of RNA synthesis (RRS) after UV irradiation due to defective preferential repair of DNA damage in actively transcribing genes, although unscheduled DNA repair is normal. The cellular findings are consistent with a defect in transcription-coupled nucleotide excision repair (TC-NER) of UV damage (summary by Itoh et al., 1994 and Nakazawa et al., 2012).For a general phenotypic description and a discussion of genetic heterogeneity of UVSS, see UVSS1 (OMIM ).Related symptoms:
- Abnormality of the nervous system
- Dry skin
More info about UV-SENSITIVE SYNDROME 3; UVSS3
Low match ATROPHODERMA VERMICULATA
Atrophoderma vermiculata, a form of keratosis pilaris atrophicans, typically presents in childhood with erythema and follicular keratotic papules that slowly progress to characteristic atrophy, which has been described as worm-eaten, reticular, or honeycomb, and occurs on the cheeks, preauricular area, and forehead. More rarely, the atrophy may extend to the upper lip, helices, ear lobes, and, in some cases, the limbs. The degree of inflammation, the presence of milia, and the extent of follicular plugs are variable (summary by Luria and Conologue, 2009).
ATROPHODERMA VERMICULATA Is also known as atrophodermia reticulata symmetrica faciei|folliculitis ulerythematosa reticulate|honeycomb atrophy|folliculitis ulerythematosa reticulata|atrophodermia vermiculataRelated symptoms:
More info about ATROPHODERMA VERMICULATA
Other less relevant matches:
Low match CLASSIC MYCOSIS FUNGOIDES
Classical mycosis fungoides is the most common type of mycosis fungoides (MF; see this term), a form of cutaneous T-cell lymphoma, and is characterized by slow progression from patches to more infiltrated plaques and eventually to tumors.
CLASSIC MYCOSIS FUNGOIDES Is also known as mycosis fungoides, alibert-bazin typeRelated symptoms:
More info about CLASSIC MYCOSIS FUNGOIDES
Palmoplantar keratoderma (PPK) is a complex group of hereditary syndromes that have been classified into diffuse, punctate, and focal forms according to the pattern of hyperkeratosis on the palms and soles (Lucker et al., 1994).For a discussion of phenotypic and genetic heterogeneity of palmoplantar keratoderma, see epidermolytic PPK (OMIM ).
PALMOPLANTAR KERATODERMA-ESOPHAGEAL CARCINOMA SYNDROME Is also known as howell-evans syndrome|keratosis palmaris et plantaris with esophageal cancer|palmoplantar hyperkeratosis-esophageal carcinoma syndrome|palmoplantar keratoderma with esophageal cancer|tylosis-oesophageal carcinoma syndrome|bennion-patterson syndrome|keratoRelated symptoms:
More info about PALMOPLANTAR KERATODERMA-ESOPHAGEAL CARCINOMA SYNDROME
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 toRelated symptoms:
More info about KAPOSI SARCOMA
Low match AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME
Autoimmune lymphoproliferative syndrome (ALPS) is a rare, inherited disorder characterized by non-malignant lymphoproliferation, multilineage cytopenias, and a lifelong increased risk of Hodgkin's and non-Hodgkin's lymphoma.
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME Is also known as alps|autoimmune lymphoproliferative syndrome, type i, autosomal dominant|fas deficiency|canale-smith syndromeRelated symptoms:
More info about AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME
Monocytopenia with susceptibility to infections is a rare, genetic, primary immunodeficiency disorder characterized by profound circulating monocytopenia, B- and NK-cell lymphopenia and severe dentritic cell decrease, which manifests clinically with disseminated mycobacterial and viral infections, as well as opportunistic fungal and parasitic infections and frequent pulmonary alveolar proteinosis. Predisposition to developping myeloid neoplasms is associated.
MONOCYTOPENIA WITH SUSCEPTIBILITY TO INFECTIONS Is also known as dendritic cell, monocyte, b and nk lymphoid deficiency|dcml|dendritic cell, monocyte, b lymphocyte, and natural killer lymphocyte deficiency|monocytopenia with susceptibility to mycobacterial, fungal, and papillomavirus infections and myelodysplasia|monocRelated symptoms:
- Hearing impairment
- Sensorineural hearing impairment
More info about MONOCYTOPENIA WITH SUSCEPTIBILITY TO INFECTIONS
Low match SÉZARY SYNDROME
Sézary syndrome (SS) is an aggressive form of cutaneous T-cell lymphoma characterized by a triad of erythroderma, lymphadenopathy and circulating atypical lymphocytes (Sézary cells).
SÉZARY SYNDROME Is also known as sÉzary lymphomaRelated symptoms:
- Abnormal facial shape
- Peripheral neuropathy
More info about SÉZARY SYNDROME
Low match FAMILIAL ATRIAL MYXOMA
Familial atrial myxoma is a rare, genetic cardiac tumor characterized by the presence of a primary, benign, gelatinous mass located in the atria and composed of primitive connective tissue cells and stroma (resembling mesenchyme) in several members of a family. Clinical presentation depends on the size, mobility and location of tumor, ranging from nonspecific and/or constitutional symptoms to sudden cardiac death, and includes dyspnea, hemoptisis, syncope, fatigue, fever, cutaneous rash, increases in venous pressure and/or peripheral edema.
FAMILIAL ATRIAL MYXOMA Is also known as atrial myxoma, familialRelated symptoms:
- Cognitive impairment
- Atrial septal defect
- Congestive heart failure
More info about FAMILIAL ATRIAL MYXOMA
Top 5 symptoms//phenotypes associated to Edema and Neoplasm of the skin
|Symptoms // Phenotype||% cases|
|Neoplasm||Uncommon - Between 30% and 50% cases|
|Lymphoma||Uncommon - Between 30% and 50% cases|
|Lymphadenopathy||Uncommon - Between 30% and 50% cases|
|Hepatomegaly||Uncommon - Between 30% and 50% cases|
|Skin rash||Uncommon - Between 30% and 50% cases|
Other less frequent symptoms
Patients with Edema and Neoplasm of the skin. may also develop some of the following symptoms:
Uncommon Symptoms - Between 30% and 50% casesHyperkeratosis Immunodeficiency Weight loss Splenomegaly Fever Alopecia Dry skin Erythema
Rare Symptoms - Less than 30% casesIrregular hyperpigmentation Hypertension Hepatosplenomegaly T-cell lymphoma Skin plaque Abnormal lymphocyte morphology Dilatation Anemia Carcinoma Palmoplantar keratoderma Ascites Gastrointestinal hemorrhage Thickened skin Lymphedema Pulmonary arterial hypertension Pneumonia Erythroderma Cutaneous T-cell lymphoma Telangiectasia Follicular hyperkeratosis Papule Eczema Epidermal acanthosis Leukemia Hypotrichosis Pruritus Severe sensorineural hearing impairment Bone marrow hypocellularity Spontaneous abortion Leukopenia Venous thrombosis Myelodysplasia Myeloid leukemia Acute myeloid leukemia Aplastic anemia Increased proportion of HLA DR+ T cells Recurrent otitis media Autoimmune neutropenia Recurrent viral infections Reduced delayed hypersensitivity Verrucae Increased IgA level B lymphocytopenia Recurrent fungal infections Lymphopenia Nephrotic syndrome Pancytopenia Platelet antibody positive Increased IgM level Sensorineural hearing impairment Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells Smooth muscle antibody positivity Antineutrophil antibody positivity Decreased lymphocyte apoptosis Recurrent infections Hypothyroidism Coombs-positive hemolytic anemia Follicular hyperplasia Rheumatoid factor positive Neutropenia Hearing impairment Decreased antibody level in blood Intermediate uveitis Antiphospholipid antibody positivity Cervical lymphadenopathy Increased IgG level Otitis media Gangrene Panniculitis Exertional dyspnea Chest pain Syncope Mitral valve prolapse Cardiomegaly Cholestasis Ischemic stroke Easy fatigability Heart murmur Tricuspid regurgitation Cerebral hemorrhage Thromboembolism Abnormality of skin pigmentation Dilatation of the cerebral artery Growth hormone excess Subarachnoid hemorrhage Edema of the lower limbs Pulmonary edema Endocarditis Orthopnea Increased inflammatory response Bacterial endocarditis Cardiac myxoma Coma Confusion Alveolar proteinosis Abnormality of the face Severe viral infections Chronic myelomonocytic leukemia Monocytopenia Recurrent mycobacterium avium complex infections Abnormal natural killer cell morphology Abnormal facial shape Peripheral neuropathy Skeletal muscle atrophy Tremor Nail dystrophy Ectropion Jaundice Lymphocytosis Abnormality of the pleura Lichenification Abnormal immunoglobulin level Seizures Cognitive impairment Atrial septal defect Congestive heart failure Behavioral abnormality Headache Chronic noninfectious lymphadenopathy Hemolytic anemia Extramedullary hematopoiesis Poor appetite Gastroesophageal reflux Nausea and vomiting Postural instability Ectodermal dysplasia Palmoplantar hyperkeratosis Poor suck Oral-pharyngeal dysphagia Squamous cell carcinoma Parakeratosis Dysphagia Abnormality of the mouth Hiatus hernia Esophagitis Oral leukoplakia Hypergranulosis Stomach cancer Esophageal stricture Plantar hyperkeratosis Clubbing of toes Hernia Abnormality of bone marrow cell morphology Diffuse palmoplantar hyperkeratosis Milia Abnormality of the nervous system Cutaneous photosensitivity Freckling Increased cellular sensitivity to UV light Pigmentation anomalies of sun-exposed skin Scarring Falls Abnormality of the cardiovascular system Acne Neurofibromas Poikiloderma Leukonychia Folliculitis Perifollicular fibrosis Atrophodermia vermiculata Skin ulcer Abnormality of the nail Hypopigmented skin patches Psoriasiform dermatitis Abnormal eyelid morphology Abnormality of the mediastinum Esophageal neoplasm Chronic lymphatic leukemia Petechiae Thrombocytopenia Autoimmunity Hepatitis Vasculitis Purpura Eosinophilia Urticaria Glomerulonephritis Increased antibody level in blood Basal cell carcinoma Neoplasm by anatomical site Autoimmune hemolytic anemia Iron deficiency anemia Hodgkin lymphoma Autoimmune thrombocytopenia Uveitis Hepatocellular carcinoma Antinuclear antibody positivity Multiple myeloma Generalized edema Renal insufficiency Susceptibility to herpesvirus Esophageal carcinoma Sarcoma Abnormality of esophagus physiology Abnormal large intestine morphology Esophageal leukoplakia Fatigue Diarrhea Encephalopathy Abnormality of the liver Abnormal lung morphology Hemangioma Hypermelanotic macule Generalized lymphadenopathy Abnormal retinal morphology Macule Abnormality of the gastrointestinal tract Abnormality of the lower limb Lymphoproliferative disorder Abnormality of the spleen Cellular immunodeficiency Skin nodule Venous insufficiency Pulmonic valve myxoma
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Frontal bossing and Protruding ear, related diseases and genetic alterations Abnormality of the skeletal system and Short metacarpal, related diseases and genetic alterations Congestive heart failure and Hemolytic anemia, related diseases and genetic alterations