Lymphatic filariasis

Lymphatic filariasis (LF) is a severe form of filariasis (see this term), caused by the parasitic worms <i>Wuchereria bancrofti</i>, <i>Brugia malayi</i> and <i>Brugia timori</i>, and the most common cause of acquired lymphedema worldwide. LF is endemic to tropical and subtropical regions. The vast majority of infected patients are asymptomatic but it can also cause a variety of clinical manifestations, including limb lymphedema, genital anomalies (hydrocele, chylocele), elephantiasis in later stages of the disease (frequently in the lower extremities), and tropical pulmonary eosinophilia (nocturnal paroxysmal cough and wheezing, weight loss, low-grade fever, adenopathy, and pronounced blood eosinophilia). Renal involvement (hematuria, proteinuria, nephritic syndrome, glomerulonephritis), and mono-arthritis of the knee or ankle joint have also been reported.



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Narrow down the case reports



Total: 45 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(4.0%)
28712247
Filariasis Presenting As Bone Marrow Suppression.
Singh A, Kumari S.
J Ayub Med Coll Abbottabad. 2016;28(3):609-610.
Pancytopenia
Animals Bone Marrow Filaria bancrofti Filariasis Homo sapiens India Male Microfilaria Pancytopenia Young Adult
1
(4.0%)
28367033
(5320880)
Microfilaria in pleural fluid cytology: A rare finding.
Pal S, Bose K, Sharma A, Sikder M.
J Lab Physicians. 2017;9(2):143-144.
Pleural effusion
1
(4.0%)
28182075
(5259929)
Coexistence of microfilaria with metastatic adenocarcinomatous deposit from breast in axillary lymph node cytology: A rare association.
Sahoo N, Saha A, Mishra P.
J Cytol. 2017;34(1):43-45.
Carcinoma
1
(4.0%)
27875706
Filariasis in Mandible and Maxilla: A Rare Entity-First Report of a Case.
Lenka S, Panda NK, Mishra S, Rathor K.
J Oral Maxillofac Surg. 2017;75(4):769.e1-769.e4.
Granuloma
Adult Combined Modality Therapy Differential Diagnosis Filarial Elephantiases Homo sapiens Imaging, Three-Dimensional Male Mandible Maxilla X-Ray Computed Tomography
1
(4.0%)
27142269
(4855865)
Microfilariae in a bone marrow aspirate.
Tummidi S, Patro MK, Bal AK, Choudhury A.
BMC Res Notes. 2016;9:256.
Eosinophilia
Animals Bone Marrow Females Filaria bancrofti Homo sapiens India
1
(4.0%)
26879053
(4754835)
Diagnosis of a malayan filariasis case using a shotgun diagnostic metagenomics assay.
Gao D, Yu Q, Wang G, Wang G, Xiong F.
Parasit Vectors. 2016;9:86.
Erythema
Animals Asians Brugia malayi DNA, Helminth Filariasis Homo sapiens Metagenomics Sequence Analysis, DNA
1
(4.0%)
26865993
(4740354)
An unusual presentation of filariasis in a nonendemic country.
Kandalam PT, Parampath AN, Farghaly HI, Salah SA, Kayakkool MK, Mathew JV, Radhakrishnan P, Al Badawi I, Farook S.
Qatar Med J. 2015;2015(2):17.
Eosinophilia
1
(4.0%)
26012217
Illness anxiety disorder related to filariasis: a case report.
Karia S, Shah N, Sonavane S, De Sousa A.
J Egypt Soc Parasitol. 2015;45(1):43-6.
Anxiety
Anxiety Disorders Filarial Elephantiases Homo sapiens Male Young Adult
1
(4.0%)
25538391
(4274533)
Incidental diagnosis of filariasis in association with carcinoma of gall bladder: Report of a case evidenced on ultrasound-guided fine-needle aspiration cytology with review of the literature.
Sinha R, Sengupta S, Pal S, Adhikari A.
J Cytol. 2014;31(3):174-5.
Neoplasm
1
(4.0%)
25298612
(4178344)
Incidental detection of microfilariae in a lymph node aspirate: A case report.
Sabageh D, Oguntola AS, Oguntola AM, Bajowa OO.
Niger Med J. 2014;55(5):438-40.
Eosinophilia
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 11

HPO ID Term # of case reports
HP:0001880 Eosinophilia 2
HP:0000100 Nephrotic syndrome 1
HP:0000618 Blindness 1
HP:0000739 Anxiety 1
HP:0001744 Splenomegaly 1
HP:0001945 Fever 1
HP:0002202 Pleural effusion 1
HP:0002716 Lymphadenopathy 1
HP:0002835 Aspiration 1
HP:0002840 Lymphadenitis 1
HP:0025289 Cervical lymphadenopathy 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID