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Gardner fibroma with localized hypertrichosis without adenomatous polyposis coli gene mutation

Yao, Xue-Yan1; Wen, Guang-Dong1; Che, Dong-Dong2; Shen, Dan-Hua3; Zhang, Jiang-Zhong1; Zhou, Cheng1

Section Editor(s): Lyu, Peng

doi: 10.1097/CM9.0000000000000383

1Department of Dermatology, Peking University People's Hospital, Beijing 100044, China

2Department of Ultrasound, Peking University People's Hospital, Beijing 100044, China

3Department of Pathology, Peking University People's Hospital, Beijing 100044, China.

Correspondence to: Dr. Cheng Zhou, Department of Dermatology, Peking University People's Hospital, Beijing 100044, ChinaE-Mail:

How to cite this article: Yao XY, Wen GD, Che DD, Shen DH, Zhang JZ, Zhou C. Gardner fibroma with localized hypertrichosis without adenomatous polyposis coli gene mutation. Chin Med J 2019;00:00–00. doi: 10.1097/CM9.0000000000000383

Received 12 June, 2019

Online date: August 09, 2019

This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.

To the Editor: Gardner fibroma (GAF)[1] is usually companied by familial adenomatous polyposis (FAP), which is related to mutations in adenomatous polyposis coli (APC).[2–4] Both GAF and FAP present with signs of Gardner syndrome (GS), triad of intestinal polyposis, soft tissue tumor (including GAF and desmoid), and osteomas.[2–4] Here, we presented a man who was diagnosed with sporadic GAF without APC gene mutations. In addition, a tubular adenoma was revealed in his sigmoid. We confirmed the significance of GAF as a powerful sentinel element for gastrointestinal organ and bone problems with or without APC mutations.[3]

The 29-year-old Chinese man complained of a painless mass on the right lateral thigh for 5 years. No significant family history was observed. Physical examination [Figure 1A] showed a soft mass with terminal hairs. In serum, the level of neuron-specific enolase was 20.4 (0–16.3) ng/mL. Gray-scale ultrasound analysis showed a superficial, ill-defined hypoechoic nodular area measuring 21 mm × 6 mm. Multiple strips of hypoechogenicity and punctated hyperechogenicity were observed in the mass. Color power Doppler analysis showed a twinkling artifact in the nodule. Histopathologic examination [Figure 1B] demonstrated the proliferation of haphazardly arranged coarse collagen fibers and an increased number of hair follicles. Immunohistochemically, β-catenin, cyclin-dependent kinases D1 (cyclin-D1), cellular myelocytomatosis (C-myc), cluster of differentiation 34 (CD34), S-100, and fibroblast growth factor 3 were negative. No abnormalities were observed on whole body bone imaging. Intra-abdominal fibroma or desmoid tumors were excluded by abdominal ultrasound. A tubular adenoma measuring 0.5 cm × 0.5 cm with low-grade dysplasia was observed in his sigmoid. Peripheral blood was collected and DNA was extracted from the patient and his parents. All 15 exons and flanking introns of the APC gene were amplified by polymerase chain reaction. However, no mutations were identified.

Figure 1

Figure 1

GAF clinically manifests as painless single or multiple sub-cutaneous masses on the back, paraspinal region, and upper extremities.[1] The diameter of the masses ranged from 0.5 to 2.5 cm. GAF occurs in individuals with or without mutations in APC.[2,3] Dahl et al[2] demonstrated that in general, GAFs with positive APC mutations were too multifocal and too large to be resected. In addition, patients with negative APC testing had a sporadic resectable GAF. GAF is diagnosed histopathologically with formless sheets of thick, haphazardly-arranged collagen bundles with interspersed fibroblasts, and a plaque-like growth pattern with infiltration and entrapment of surrounding structures. Immunohistochemically, β-catenin, cyclin-D1, c-myc, and CD34 reactivity were also noted in GAF.[2] Over-expression of β-catenin and cyclin-D1 can be caused by an abnormal APC gene.[2,5]

Mutations in the APC gene[1,4] may lead to GS, FAP, or GAF.[3] However, in some rare cases, sporadic GAF without APC mutations can develop FAP.[2] Therefore, GAF may serve as a powerful sentinel element for internal organ and bone problems with or without APC mutations. Taken together, patients with GAF should undergo comprehensive examinations combined with genetic mutation testing. Here, we also highlighted localized hypertrichosis as a special manifestation in our case, which may indicate a relationship between fibrous proliferation and the formation of hair follicles in GAF. Further studies will be required.

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Declaration of patient consent

The authors certify that they have obtained all necessary patient consent forms, stating that the patient has consented to the use of his clinical information for publication in the journal. The patient understands that his name and initials will not be published, and due efforts will be made to conceal the identity, but anonymity cannot be guaranteed.

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This work was supported by grants from the National Natural Science Foundation of China (No. 81402588 and 81773311).

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Conflicts of interest


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