# Bizarre parosteal osteochondromatous proliferation in the distal ulna where the lesion is continuous with the medullary cavity: a case report

**Authors:** Tianyu Wang, Zhengxiao Ouyang, Zhuzhong Chen, Yuhui Yang, Xiaoyi Huang, Cheng Xiang, Lin Ling, Peng Zhou, Xiaoning Guo

PMC · DOI: 10.1186/s12891-024-07715-4 · BMC Musculoskeletal Disorders · 2024-07-26

## TL;DR

A rare case of BPOP in a child's ulna showed unusual continuity with the medullary cavity, requiring careful surgical removal to prevent recurrence.

## Contribution

This case report highlights an atypical BPOP with medullary cavity continuity, expanding understanding of its clinical presentation and management.

## Key findings

- The BPOP lesion was continuous with the medullary cavity, an atypical feature compared to most cases.
- Surgical resection with adequate margins improved forearm function and prevented recurrence in the 1-year follow-up.
- Recognition of rare BPOP features is crucial to avoid misdiagnosis and ensure appropriate treatment.

## Abstract

Bizarre parosteal osteochondromatous proliferation (BPOP) is a rare benign bone tumor, it is also called “Nora’s lesion”. The lesion is characterized by heterotopic ossification of the normal bone cortex or parosteal bone. The etiology of BPOP is unclear and may be related to trauma. In most BPOPs, the lesion is not connected to the medullary cavity. Here we report an atypical case, characterized by reversed features compared to the typical BPOP, which demonstrated continuity of the lesion with the cavity.

An 11-year-old female child had a slow-growing mass on her right wrist for 8 months with forearm rotation dysfunction. Plain X-rays showed an irregular calcified mass on the right distal ulna, and computed tomography (CT) showed a pedunculated mass resembling a mushroom protruding into the soft tissue at the distal ulna. The medulla of this lesion is continuous with the medulla of the ulna. A surgical resection of the lesion, together with a portion of the ulnar bone cortex below the tumor was performed, and the final pathology confirmed BPOP. After the surgery, the child’s forearm rotation function improved significantly, and there was no sign of a recurrence at 1-year follow-up.

It is scarce for BPOP lesions to communicate with the medullary cavity. However, under-recognition of these rare cases may result in misdiagnosis or inappropriate treatment thereby increasing the risk of recurrence. Therefore, special cases where BPOP lesions are continuous with the medulla are even more important to be studied to understand better and master these lesions. Although BPOP is a benign tumor with no evidence of malignant transformation, the recurrence rate of surgical resection is high. We considered the possibility of this particular disease prior to surgery and performed a surgical resection with adequate safety margins. Regular postoperative follow-up is of utmost importance, without a doubt.

## Linked entities

- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** forearm rotation dysfunction (MESH:D005543), trauma (MESH:D014947), BPOP (MESH:C565054), heterotopic ossification of the normal bone (MESH:D009999), benign tumor (MESH:D009369), benign bone tumor (MESH:D001859), Nora's lesion (MESH:D009059)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11282834/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11282834/full.md

---
Source: https://tomesphere.com/paper/PMC11282834