# Autosplenectomy in a Patient With Autoimmune Polyglandular Syndrome Type 2 (APS‐2)

**Authors:** Luqman S. Fauzi, Airin Jyoty, Yashwin Sredharan, Manohara Kenchaiah

PMC · DOI: 10.1155/crie/6610410 · Case Reports in Endocrinology · 2026-01-28

## TL;DR

A rare case of autoimmune polyglandular syndrome type 2 (APS-2) is reported where the patient experienced complete spleen atrophy, likely due to an autoimmune cause.

## Contribution

This is the first reported case of APS-2 associated with autosplenectomy, highlighting a new clinical consideration for the syndrome.

## Key findings

- The patient showed progressive splenic atrophy over seven years, leading to anatomical asplenia.
- The splenic dysfunction is hypothesized to be autoimmune in origin, unlike previously known APS-1 cases.
- The case emphasizes the need for long-term monitoring of splenic function in APS patients.

## Abstract

Autoimmune glandular syndrome type 2 is a complex genetic condition where a triad of endocrinopathies is involved, namely, Addison’s disease, type 1 diabetes, and/or autoimmune thyroid disorder. The disease predisposes one to a variety of other autoimmune associations. Here, we report a rare presentation of a patient with autoimmune polyglandular syndrome type 2 (APS‐2) presenting with a 7‐year history of progressive splenic atrophy causing functional hyposplenism that ultimately progressed to anatomical asplenia (autosplenectomy) as demonstrated in the serial imaging. We postulate that the underlying cause of this presentation is also of autoimmune nature. Unlike APS‐1, which has been linked to hyposplenism, this is the first reported case of APS‐2 with similar splenic involvement. Splenic hypofunction can increase susceptibility to encapsulated bacterial infection, with overwhelming postsplenectomy infection (OPSI) being a significant threat. It is crucial that clinicians recognize the importance of providing guidance on vaccinations, antibiotic chemoprophylaxis, and patient education for individuals with asplenia or hyposplenism. If patients with APS can experience progressive splenic atrophy, we suggest long‐term follow‐up with splenic function assessment. It is yet unclear whether preemptive screening with pitted red cell count has any clinical impact in this group of patients.

## Linked entities

- **Diseases:** Addison’s disease (MONDO:0100480), type 1 diabetes (MONDO:0005147), autoimmune polyglandular syndrome type 2 (MONDO:0010012)

## Full-text entities

- **Diseases:** autoimmune (MESH:D001327), OPSI (MESH:D007239), autoimmune thyroid disorder (MESH:D013967), bacterial infection (MESH:D001424), splenic atrophy (MESH:D013158), type 1 diabetes (MESH:D003922), Addison's disease (MESH:D000224), asplenia (MESH:D059446), APS (MESH:D016884), Splenic hypofunction (MESH:D000309), endocrinopathies (MESH:C567425), Autoimmune glandular syndrome type 2 (MESH:D000081012)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12849194/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12849194/full.md

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Source: https://tomesphere.com/paper/PMC12849194