Langerhans cell histiocytosis presenting as post-COVID-19 multisystem inflammatory syndrome: A rare case report
Langerhans cell histiocytosis is a rare clonal disease of monocyte-macrophage system characterized with uncontrolled proliferation and accumulation of immature dendritic cells. Acute disseminated form of this disease known as Letterer-Siwe disease is life threatening. Here, we report such a case who...
Saved in:
Main Authors: | K M Sudhakar Rao (Author), Varsha R Koti (Author), Balachandra Suryakant Ankad (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2022-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Multisystem langerhans cell histiocytosis in adult
by: Anubhav Garg, et al.
Published: (2012) -
Multisystemic Langerhans cell histiocytosis in an adult
by: Marie-Valerie Hegemann, MD, et al.
Published: (2017) -
Multifocal multisystem Langerhans cell histiocytosis
by: Anupam Das, et al.
Published: (2017) -
Langerhans cell histiocytosis: a rare case of the multisystemic form in an infant
by: Thaís Oliveira Utiyama, et al.
Published: (2023) -
Multisystemic Langerhans cell histiocytosis: case report
by: Larissa A. Paiva, et al.