Discussion and conclusions
The term “mesenchymal hamartoma” was first proposed in 1979 by McLeod and Dahlin, as it best reflected the benign nature of this lesion composed of disordered but non-neoplastic skeletal tissues [
3]. Odell and Benjamin were the first to use the term “mesenchymal hamartoma of the chest wall” in 1986 [
4]. Its incidence is estimated to be 1 in 3000 among primary bone tumors or less than 1 per million in the general population [
5]. Approximately 100 cases have been described to date, most occurring prenatally or within the first 6 months of life [
6]. To the best of our knowledge, only two cases of chondromesenchymal hamartoma have been reported in adults. Bilateral multifocal lesions (CT revealed three masses on the right side and two masses on the left side) were discovered in a 47-year-old man who did not undergo treatment until 13 years later when he developed chest pain [
7]. Another asymptomatic left chest wall tumor was discovered incidentally during a complete medical checkup in a 39-year-old woman. The tumor was excised
en bloc with segments of the 7th and 8th ribs [
8]. The age of onset in our case (24 years old) is also quite uncommon, making this only the third adult patient with chondromesenchymal hamartoma reported worldwide.
Chondromesenchymal hamartomas are usually unilateral and are commonly seen on the right side, with a male-to-female ratio of 1.6:1 [
9]. A few cases of bilateral lesions have also been reported [
1,
7,
10]. Typically, these lesions arise from one or several ribs and their size may range from a few to a dozen centimeters. In most cases, these lesions occur in isolation; however, they are occasionally multifocal [
7,
11,
12]. Patients may present with respiratory distress or be asymptomatic. Less common manifestations include scoliosis, chest wall deformity, cough, and fever [
1]. One infant died 14 days after birth of severe sepsis secondary to
Pseudomonas aeruginosa infection and pulmonary insufficiency [
13]. Patient 2 in this report is the first documented instance of DIC as a postoperative complication following excision of chondromesenchymal hamartoma. Although this complication may not be directly related to this condition or its surgical treatment, it remains a possibility; therefore, we believe that assessing coagulation function preoperatively is important.
Imaging studies are helpful in determining the site of origin, tumor density, enlargement, and effect on adjacent structures; however, imaging is not considered diagnostic and may be misleading if the tumor location or patient age is atypical [
14,
15]. In patient 1, the imaging finding of a paravertebral mass in an adult appeared to mimic a posterior mediastinal tumor and the radiologist suggested the possibility of a neurogenic tumor. Malignant lesions such as congenital neuroblastoma, Ewing’s sarcoma, malignant teratoma, osteosarcoma, or chondrosarcoma cannot be excluded in the presence of cortical erosion, rib destruction, or deformation of adjacent ribs as seen on imaging [
16,
17]. Biopsy of the lesion can be complicated by severe bleeding because of disruption of the vascular spaces; therefore, needle biopsy should be performed cautiously [
1,
2].
Microscopically, chondromesenchymal hamartomas have immature spindle-shaped mesenchymal cells, plate-like hyaline cartilage, woven bone formation, endochondral ossification and calcification, osteoclastic giant cells, and secondary ABC changes; abnormal mitoses and atypia are not present [
18]. Woven trabeculae containing hematopoietic marrow are common, as observed in patient 2. Areas resembling ABC, with osteoclast-like giant cells, blood-filled spaces, hemosiderin-laden macrophages, and fibromembranous septa, are specific for chondromesenchymal hamartoma. It has been proposed that the formation of an ABC is secondary to intraosseous arteriovenous fistula formation [
19]. IHC staining may demonstrate the presence of S-100 protein in cartilaginous areas [
4]. To the best of our knowledge, no current molecular genetic tests are available to assist in the diagnosis of chondromesenchymal hamartoma [
10].
The differential diagnosis of chondromesenchymal hamartoma includes tumoral and non-tumoral lesions involving the ribs that are common in infants and children, including primary ABC, chondrosarcoma, enchondroma, osteochondroma, fibrous dysplasia, and osteofibrous dysplasia (OFD) [
14]. Primary ABC and chondromesenchymal hamartoma both show cystic areas; however, they lack solid cartilage nodules and component diversity. It is noteworthy that ABC could be secondary to various bone tumors, including giant cell tumors, chondroblastomas, fibrous histiocytomas, chondromyxoid fibromas, fibrous dysplasia, and osteosarcoma [
20]. Chondrosarcoma is primarily a tumor of adulthood and older age [
21]. It is characterized by high cellularity, presence of host bone entrapment, and absence of host bone encasement. Chondrosarcoma is characterized by mild-to-moderate atypical chondrocytes, varying in size and shape, and containing enlarged, hyperchromatic nuclei. Myxoid changes or chondroid matrix liquefaction is a common feature of chondrosarcomas [
22]. Enchondroma is a benign hyaline cartilage neoplasm arising within the medullary bone cavity; normal bone marrow elements may also be observed between its nodules, as seen in patient 2. Noticeably, enchondroma often appears as pale blue on hematoxylin and eosin staining owing to its high matrix proteoglycan content and it is less diverse in terms of histological components than chondromesenchymal hamartoma. Osteochondroma originates from the bone surface and possesses a distinctive three-layer structure of perichondrium, cartilage, and bone. The outer layer is a fibrous perichondrium that is continuous with the periosteum, below which is a hyaline cartilage cap with endochondral ossification. Similar to chondromesenchymal hamartoma, fibrous dysplasia can occur in the ribs, contain a cartilaginous component with endochondral ossification, and have secondary changes including ABC-like areas and multinucleated osteoclastic giant cells. However, fibrous dysplasia is mainly composed of bland fibroblastic cells and irregular trabeculae of woven bone; mesenchymal cells and plate-like hyaline cartilage are not its main components [
22]. OFD mostly involves cortical bone of the anterior mid-shaft of the tibia during infancy and childhood; it is composed of fragments of woven bone rimmed by lamellar bone layers laid down by well-defined osteoblasts [
22]. Although secondary ABC and multinucleated giant cells may be seen in OFD, there is an absence of cartilage. Lung hamartoma, which is the most common cartilage-containing benign lung tumor, should also be taken into consideration in the differential diagnosis. Since this tumor is composed of tissues that are normally present in the lung, the presence of normal bronchial epithelium could be a valuable clue [
23]. Unlike chondromesenchymal hamartoma, lung hamartoma is mostly found in the lung parenchyma or within the bronchus and may only secondarily involve the ribs [
24].
Molecular diagnostic techniques have recently emerged as independent diagnostic tools to improve diagnostic accuracy and reduce interobserver variability; many characteristic genetic alterations have been identified in bone tumors [
25].
USP6 and/or
CDH11 rearrangements are found in 69% of primary ABCs, but not in secondary ABC [
26].
IDH1 (R132C; R132H) or
IDH2 (R172S) mutations may occur in enchondromas, atypical cartilaginous tumor/grade 1 central chondrosarcomas, grade 2/3 central chondrosarcomas, and dedifferentiated chondrosarcomas; however, they are absent in osteochondromas [
27,
28].
MDM2 and
CDK4 are amplified in low-grade central osteosarcomas and periosteal osteosarcomas, as demonstrated by FISH/IHC [
29]. K36M mutations in
H3F3B appear in about 95% of chondroblastomas, while G34W/L mutations in
H3F3A are found in 92% of giant cell tumors of the bone [
30]. It is likely that molecular markers will increasingly play an important role in improving the diagnosis and treatment of bone tumors.
The treatment strategy for chondromesenchymal hamartoma involves one of two main approaches: conservative management for asymptomatic patients and surgical treatment for patients with respiratory distress caused by mass compression. A case of spontaneous regression of a chest wall hamartoma in an infant was reported [
31]. In most cases, surgical resection is chosen irrespective of symptoms. Secondary surgery may be required following incomplete resections [
9]. Patients with significant upper airway obstruction may need permanent tracheotomy [
32]. A third management option, radiofrequency thermoablation (RFT), a relatively noninvasive technique performed under CT guidance, was performed in a 6-month-old girl [
33]. RFT causes coagulative necrosis in the lesion, which is gradually reabsorbed. This method avoids damage to the adjacent normal bone and is well tolerated in children, thereby decreasing the risk of severe postoperative complications [
34].
Herein, we reported two extremely rare cases of chondromesenchymal hamartoma. Although the lesions in these cases were morphologically similar to previously reported cases, they had distinct radiological and clinical characteristics. To the best of our knowledge, case 1 is only the third report of an adult patient with chondromesenchymal hamartoma. This patient was suspected of having a posterior mediastinal tumor on radiology. Case 2 is the first documentation of DIC as a postoperative complication of chondromesenchymal hamartoma. This report may raise awareness regarding the presentation, diagnosis, and management of chondromesenchymal hamartoma among pathologists, radiologists, and clinicians.
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