Evidence map›Paper›PMID 42851894›Full record

ArticleJournal of orthopaedic case reports2026

Multimodal Biological Augmentation with Umbilical Cord Mesenchymal Stem Cell Secretome, Recombinant Human Bone Morphogenetic Protein-2, and Allogeneic Umbilical Cord Mesenchymal Stem Cells in Neurofibromatosis Type 1-Confirmed Congenital Pseudarthrosis of the Distal Tibia and Fibula: A Case Report with Mechanistic Scoping Review.

Luh Gede Djatu Anggitadewi, Oen Sindrawati, Komang Agung Irianto, Tri Wahyu Martanto

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In one paragraph

Article in Journal of orthopaedic case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Luh Gede Djatu AnggitadewiDepartment of Orthopaedics and Traumatology, Dr. Soetomo General Academic Hospital/Faculty of Medicine, Airlangga University, Surabaya, Indonesia.
Oen SindrawatiDepartment of Orthopaedics and Traumatology, Surabaya Orthopaedics and Traumatology Hospital, Surabaya, Indonesia.
Komang Agung IriantoDepartment of Orthopaedics and Traumatology, Dr. Soetomo General Academic Hospital/Faculty of Medicine, Airlangga University, Surabaya, Indonesia.
Tri Wahyu MartantoDepartment of Orthopaedics and Traumatology, Dr. Soetomo General Academic Hospital/Faculty of Medicine, Airlangga University, Surabaya, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Congenital pseudarthrosis of the tibia (CPT) associated with neurofibromatosis type 1 (NF1) is characterized by convergent dysregulation of three molecular pathways - transforming growth factor-beta/Smad-driven fibrogenesis, RAS-MEK-ERK hyperactivation, and Wnt/β-catenin blockade - none of which is addressed by conventional surgical fixation alone. This case explores the clinical feasibility of a multimodal biological protocol targeting all three pathways simultaneously. Case Report: A 6-year-old male with histopathologically confirmed NF1-associated Crawford type IV CPT of the distal tibia and concurrent distal fibular pseudarthrosis underwent radical hamartoma excision combined with quadruple biological augmentation: Allogeneic umbilical cord mesenchymal stem cells (UC-MSC) (20 million cells), UC-MSC conditioned medium (secretome; first injection intraoperatively post-graft), recombinant human bone morphogenetic protein-2 (rhBMP-2) (Novosys), and synthetic hydroxyapatite scaffold (Bongros), stabilized with an Ilizarov trans-ankle external fixator. A second secretome injection (1.4 mL, fluoroscopy-guided) was administered percutaneously at 8 months, targeting the distal tibial union site during frame removal. Conclusion: Tibial callus measured 9.88 mm at 6 months (equalling diaphyseal width) with no graft resorption. At 8 months, tibial bridging callus was sufficient to permit Ilizarov frame removal without refracture. The distal tibial pseudarthrosis was stabilized with retained K-wires; the fibula received no internal fixation and showed no ongoing healing. No infection or hardware complication occurred. This case is, to our knowledge, the first to describe this quadruple augmentation protocol and a two-stage secretome delivery strategy in CPT, providing a hypothesis-generating proof of concept for future translational investigation.

Indexed as

Congenital pseudarthrosis tibiaIlizarovmesenchymal stem cell secretomeneurofibromatosis type 1recombinant bone morphogenetic protein-2

Identifiers

PMID42851894
PMCPMC13646567

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.