Autoimmune lymphoproliferative syndrome natural history, complications and prognosis: Difference between revisions
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===Natural History=== | ===Natural History=== | ||
*The symptoms of | *The symptoms of [[Autoimmune lymphoproliferative syndrome]] usually develop in the first decade of life and start with [[symptoms]] such as [[splenomegaly]], [[lymphadenopathy]] and [[cytopenia]].<ref name="BrideTeachey2017">{{cite journal|last1=Bride|first1=Karen|last2=Teachey|first2=David|title=Autoimmune lymphoproliferative syndrome: more than a FAScinating disease|journal=F1000Research|volume=6|year=2017|pages=1928|issn=2046-1402|doi=10.12688/f1000research.11545.1}}</ref><ref name="ShahWu2014">{{cite journal|last1=Shah|first1=Shaili|last2=Wu|first2=Eveline|last3=Rao|first3=V. Koneti|last4=Tarrant|first4=Teresa K.|title=Autoimmune Lymphoproliferative Syndrome: an Update and Review of the Literature|journal=Current Allergy and Asthma Reports|volume=14|issue=9|year=2014|issn=1529-7322|doi=10.1007/s11882-014-0462-4}}</ref> | ||
===Complications=== | ===Complications=== |
Revision as of 04:44, 26 June 2021
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
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Overview
If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
OR
Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
OR
Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [#]%.
Natural History, Complications, and Prognosis
Natural History
- The symptoms of Autoimmune lymphoproliferative syndrome usually develop in the first decade of life and start with symptoms such as splenomegaly, lymphadenopathy and cytopenia.[1][2]
Complications
- Common complications of [disease name] include:
- [Complication 1]
- [Complication 2]
- [Complication 3]
Prognosis
- Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [--]%.
- Depending on the extent of the [tumor/disease progression] at the time of diagnosis, the prognosis may vary. However, the prognosis is generally regarded as poor/good/excellent.
- The presence of [characteristic of disease] is associated with a particularly [good/poor] prognosis among patients with [disease/malignancy].
- [Subtype of disease/malignancy] is associated with the most favorable prognosis.
- The prognosis varies with the [characteristic] of tumor; [subtype of disease/malignancy] have the most favorable prognosis.
References
- ↑ Bride, Karen; Teachey, David (2017). "Autoimmune lymphoproliferative syndrome: more than a FAScinating disease". F1000Research. 6: 1928. doi:10.12688/f1000research.11545.1. ISSN 2046-1402.
- ↑ Shah, Shaili; Wu, Eveline; Rao, V. Koneti; Tarrant, Teresa K. (2014). "Autoimmune Lymphoproliferative Syndrome: an Update and Review of the Literature". Current Allergy and Asthma Reports. 14 (9). doi:10.1007/s11882-014-0462-4. ISSN 1529-7322.