A case report of hand, foot, and mouth disease with necrotizing mucocutaneous lesions

Purpose: To report the case of a 33-year old man who disclosed the first case of bilateral ocular involvement of hand, foot, and mouth disease (HFMD) with a different stage of the disease in each eye. Methods: Retrospective case report. Results: The study included a patient who incurred in a bilateral HFMD maculopathy. During 6 months follow-up period persistent abnormalities in fundus examination and in OCT scans were reported. Conclusion: We consider that our case shows that choriocapillaris is the primary target of HFMD maculopathy, for this reason we consider that ICGA is mandatory for early diagnosis and an effective treatment.

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Hand, foot and mouth disease - a short case report

Journal of Clinical and Experimental Dentistry ◽

10.4317/jced.52031 ◽

2015 ◽

pp. e336-e338 ◽

Cited By ~ 3

Author(s):

RR Kashyap ◽

RS Kashyap

Keyword(s):

Case Report ◽

Foot And Mouth Disease ◽

Mouth Disease ◽

Foot And Mouth

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Secondary hypogonadism following hand, foot, and mouth disease in an adult: a case report and review of literature

BMC Infectious Diseases ◽

10.1186/s12879-022-07030-0 ◽

2022 ◽

Vol 22 (1) ◽

Author(s):

Zhaoying Chen ◽

Chen Jiang ◽

Xiaoyu Cheng ◽

Lidan Ma ◽

Ying Xin ◽

...

Keyword(s):

Erectile Dysfunction ◽

Case Report ◽

Foot And Mouth Disease ◽

Psychological Trauma ◽

Mouth Disease ◽

Case Presentation ◽

Immunodeficiency Virus ◽

Foot And Mouth ◽

History Of ◽

Secondary Hypogonadism

Abstract Background Previous reports have described hypogonadism associated with virus infection such as hantavirus, human immunodeficiency virus (HIV) or severe acute respiratory syndrome coronavirus 2 (SARS-COV-2). However, to our best knowledge there has been no case report of secondary hypogonadism following hand, foot, and mouth disease (HFMD). Case presentation A previously healthy 28-year-old man with no history of major physical and psychological trauma, presented with bilateral gynecomastia and erectile dysfunction 2 weeks after HFMD. Laboratory testament showed the level of gonadotropin hormones declined. Imaging examination demonstrated no major abnormal change in pituitary or reproductive system. The diagnosis of hypogonadism was established. Then the patient was ordered to maintain mental health outward of hospital without drug intervention. One month after presentation, his gonadotropin hormone level and sexual desire had recovered, while bilateral gynecomastia and erectile dysfunction symptoms disappeared. Conclusions Physicians should notice the possibility for hypogonadism in adult patients with a recent history of HFMD.

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Hand, foot and mouth disease in late 3rd trimester of pregnancy: A case report

Progress in Drug Discovery & Biomedical Science ◽

10.36877/pddbs.a0000056 ◽

2020 ◽

Vol 3 (1) ◽

Author(s):

Pusparajah Priyia ◽

Joanna Xuan Hui Goh ◽

Learn-Han Han ◽

Prithvy Lingham

Keyword(s):

Case Report ◽

Caesarean Section ◽

Foot And Mouth Disease ◽

Mouth Disease ◽

Foot And Mouth ◽

Hands And Feet ◽

In Pregnancy

We present a case of a 28-year-old primigravida who was diagnosed with hand, foot and mouth disease (HFMD) at 39 weeks gestation. Patient had the classical rash over her hands and feet but was otherwise well. The baby was delivered at 40 weeks via Caesarean section and was well after delivery. We discuss the literature associated with hand, foot and mouth disease in pregnancy as well as briefly discuss complications associated with the causative organisms of HFMD.

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