# Posterior Fossa Sinking Skin Flap Syndrome Presenting With Orthostatic Vertigo After Decompressive Craniectomy: A Case Report

**Authors:** Ryo Matsuzaki, Yuki Sakaeyama, Shuhei Kubota, Sayaka Terazono, Nobuo Sugo

PMC · DOI: 10.7759/cureus.101765 · Cureus · 2026-01-18

## TL;DR

A rare case of sinking skin flap syndrome after brain surgery was successfully treated with delayed cranioplasty, resolving vertigo and vomiting.

## Contribution

This case highlights SSFS as a potential cause of orthostatic vertigo after posterior fossa decompression.

## Key findings

- Symptoms worsened in upright position and improved when supine, with a visible scalp depression.
- Cranioplasty led to rapid and sustained resolution of symptoms.
- SSFS should be considered in patients with large posterior fossa defects and posture-dependent symptoms.

## Abstract

Sinking skin flap syndrome (SSFS) is an uncommon complication of cranial defects and is rarely described after posterior fossa decompression. We report a case of chronic phase posterior fossa SSFS presenting with positional vertigo and vomiting, successfully treated with delayed cranioplasty. A 40-year-old man presented with subarachnoid hemorrhage caused by a ruptured vertebral artery dissecting aneurysm involving the left posterior inferior cerebellar artery (PICA). He underwent an occipital artery (OA)-PICA bypass and trapping of the aneurysm, followed by decompressive suboccipital craniectomy without immediate cranioplasty. Progressive ventriculomegaly developed, and a ventriculoperitoneal (VP) shunt (Codman Hakim, Integra Japan, Tokyo, Japan) was placed. He was later readmitted with vertigo and vomiting that worsened in the upright position and improved when supine, accompanied by a conspicuous depression and postural change of the scalp flap over the defect. Posterior fossa SSFS was diagnosed, and cranioplasty was performed, leading to rapid and sustained symptom resolution. SSFS should be considered in patients with large posterior fossa defects who develop posture-dependent symptoms, particularly when local soft-tissue support is limited; timely cranioplasty may be therapeutic.

## Linked entities

- **Diseases:** subarachnoid hemorrhage (MONDO:0005099)

## Full-text entities

- **Diseases:** syndrome of the trephined (MESH:D013577), atrophy of the neck muscles (MESH:D009133), headaches (MESH:D006261), trauma (MESH:D014947), volume loss (MESH:D016388), atrophy (MESH:D001284), atrophic (MESH:D020966), aneurysm (MESH:D000783), brain atrophy (MESH:C566985), ischemic (MESH:D002545), artery dissecting aneurysm (MESH:D000784), hemispheric defects (MESH:D006832), vertebral artery dissecting aneurysm (MESH:D020217), Vertigo (MESH:D014717), ruptured aneurysm (MESH:D017542), stroke (MESH:D020521), CSF hypovolemia (MESH:D019585), CSF leakage (MESH:D065634), loss of subcutaneous fat and muscle mass (MESH:C536030), quadriparesis (MESH:D011782), vomiting (MESH:D014839), contracture (MESH:D003286), cranial defect (MESH:D003389), motor deficits (MESH:D009461), ischemia (MESH:D007511), cerebellar atrophy (MESH:D002526), Chiari malformation (MESH:D001139), impaired consciousness (MESH:D003244), brain (MESH:D001927), subarachnoid hemorrhage (MESH:D013345), brain parenchymal loss (MESH:D002543), dysphagia (MESH:D003680), Posterior (MESH:D001041), weight loss (MESH:D015431), bone defect (MESH:D001847), hemiparesis (MESH:D010291), dizziness (MESH:D004244), ventricular enlargement (MESH:D006332), pneumocephalus (MESH:D011007), hemiplegia (MESH:D006429), skull defect (MESH:D012888), depressed (MESH:D003866), infarction (MESH:D007238), Coma (MESH:D003128), neurological deterioration (MESH:D009422), bony (MESH:D018213), hydrocephalus (MESH:D006849), Sinking Skin Flap Syndrome (MESH:D000070600)
- **Chemicals:** VP (-), titanium (MESH:D014025)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12910409/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12910409/full.md

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Source: https://tomesphere.com/paper/PMC12910409