|Year : 2020 | Volume
| Issue : 5 | Page : 316-318
A rare case of pediatric osteochondroma presenting as hemothorax
Pavai Arunachalam1, Cenita J Sam1, K Jothi Lakshmi2, Hari Baskar Shanmugham3
1 Department of Paediatric Surgery, PSGIMS and R, Coimbatore, Tamil Nadu, India
2 Department of Paediatrics, PSGIMS and R, Coimbatore, Tamil Nadu, India
3 Department of CRRI, PSGIMS and R, Coimbatore, Tamil Nadu, India
|Date of Submission||25-Oct-2019|
|Date of Decision||14-Dec-2019|
|Date of Acceptance||11-Apr-2020|
|Date of Web Publication||1-Sep-2020|
Dr. Pavai Arunachalam
Department of Paediatric Surgery, PSGIMS and R, Coimbatore, Tamil Nadu
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Isolated osteochondroma presenting as hemothorax is a rare entity. A 7-year-old boy presented with respiratory distress and diagnosed with hemothorax, and computed tomography showed osteochondroma and removal with resection of the rib was curative.
Keywords: Curative resection, hemothorax, osteochondroma
|How to cite this article:|
Arunachalam P, Sam CJ, Lakshmi K J, Shanmugham HB. A rare case of pediatric osteochondroma presenting as hemothorax. J Indian Assoc Pediatr Surg 2020;25:316-8
|How to cite this URL:|
Arunachalam P, Sam CJ, Lakshmi K J, Shanmugham HB. A rare case of pediatric osteochondroma presenting as hemothorax. J Indian Assoc Pediatr Surg [serial online] 2020 [cited 2020 Oct 31];25:316-8. Available from: https://www.jiaps.com/text.asp?2020/25/5/316/294009
| Introduction|| |
Osteochondroma is the most common benign lesion of the bones, commonly arising from the growing end of long bones. It is characterized as bony outgrowths from the surface with a cartilaginous cap. It can be solitary or multiple, with the former most commonly seen in clinical practice. Osteochondromas are benign developmental anomalies, characterized by the separation of epiphysis growth-plate cartilage from the main epiphysis.
It is commonly seen on the long bones. However, the index child had an osteochondroma of rib presenting as hemothorax which is exceedingly rare, and hence, presented as a case report.
| Case Report|| |
The index case was a 7-year-old boy admitted with complaints of difficulty in breathing along with left-sided chest pain of 2-day duration. There was no history of trauma or infections or any other respiratory symptomatology. The child had no swelling anywhere else in the body, and the parents were normal.
The clinical examination revealed evidence of left pleural effusion. Complete blood count within normal parameters and Mantoux test was negative, and the patient reported no history of recent contact with tuberculosis patients. Coagulation profile was also normal. Chest X-ray [Figure 1] and ultrasound showed collection of moderate amounts of pleural fluid associated with collapse of the left lower lobe.
Diagnostic aspiration under ultrasound guidance revealed uniformly bloody fluid from the pleural cavity. Computed tomography (CT) of the chest [Figure 2] was done which revealed a speculated tumor mass over the left seventh rib near the anterior end, protruding toward the left lower lobe of the lung which is clearly evident upon three dimensional (3-D) reconstruction. Thus, a diagnosis of bony tumor causing perforative injury to the left lower lobe of the lung causing hemothorax was made.
|Figure 2: Three-dimensional computed tomography reconstruction showing the osteochondroma involving the anterior portion of the left seventh rib on the inner aspect|
Click here to view
The child was taken up for the surgery, and thoracoscopy was done initially to identify and localize the lesion and to rule out any complications. The bony spicule over the left seventh rib was resected, which was a 2 cm × 2 cm hard spicule with a smooth surface from the inner surface of the rib injuring the adjacent pleura and lung parenchyma.
The histopathological examination revealed nodular lesion comprising external fibrous tissue, middle cartilaginous tissue, and inner bony trabeculae enclosing the marrow cavity [Figure 3]. There was endochondral ossification with proliferating capillaries, hematopoietic and fatty marrow elements within the lesion. The outer fibrous layer is seen continuous with the periosteum of underlying bony tissue.
|Figure 3: Histopathological examination showing external fibrous tissue, middle cartilaginous tissue, and inner bony trabeculae|
Click here to view
These confirmed the diagnosis of osteochondroma of rib, in benign status.
| Discussion|| |
Being relatively common tumor of long bones, the incidence of osteochondroma of ribs is exceedingly rare, with an incidence of 1 in 50,000 only. Even rarer is the osteochondroma causing hemothorax in the pediatric age group with only <5 cases reported in previous literature. The rarity of the case was the main reason for reporting it.
Kadu et al., have previously reported a similar case of 9-year-old boy with osteochondroma of the right 6th rib. During his follow-up of 3-year period, the tumor did not increase in size or developed any complications and hence was managed conservatively.
Most of the patients are asymptomatic which makes it hard to diagnose. Only very few cases are observed with symptoms such as chest pain.
Osteochondroma starts early in childhood and grows till skeletal maturity is reached. It is asymptomatic when benign and small. The main complications include fracture of rib, vascular injury, osseous deformities, neural compression, and malignant transformation.
Our patient had a rare complication of hemothorax caused by the lesion, possibly due to chronic irritation of the chondroma spicule growing inward into the pleura, causing bleeding from pleural vessels.
The tumor peaks around the age group of 10–30 years with a 3% thoracic origin, which rises to 10% in hereditary multiple exostosis, as evident by the case report submitted by Maeda et al., where the children suffering from hereditary multiple exostosis and strong family history, eventually developed osteochondroma in the ribs at latter part of life., Hence, it is considered worthwhile to closely follow-up such patients with hereditary multiple exostosis.
Bess et al. emphasized the importance of preoperative radiological evaluation to provide optimal data about the lesions such as erosion, internal lytic areas, and destruction of adjacent structures, calcifications, and soft-tissue masses. The size of the cartilaginous cap serves as the best indicator of malignant transformation in osteochondroma.
However, according to Naidu et al., like in our index case, CT scan when coupled with reconstruction technique can help to localize the lesion, but the size is often underestimated because of cartilaginous cap, which can be better visualized by magnetic resonance imaging.
Malignant transformation of osteochondroma is very rare and has been seen only in <1% of solitary and 2% of hereditary multiple exostosis cases.
Few other adult cases of osteochondroma of rib have been reported by Phatak et al., but all of them were asymptomatic and were incidentally found, unlike our index child who presented with hemothorax due to osteochondroma.
The presence of complications favored surgical excision as the mainstay of treatment unlike previously reported cases, which were asymptomatic and hence managed conservatively.
This emphasized the importance of osteochondroma as an etiological factor in hemothorax and should be given due consideration while considering a diagnosis in the pediatric age group.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Shim JH, Park CK, Shin SH, Jeong HS, Hwang JH. Solitary osteochondroma of the twelfth rib with intraspinal extension and cord compression in a middle-aged patient. BMC Musculoskelet Disord 2012;13:57.
Tateishi U, Yamaguchi U, Miyake M, Maeda T, Chuman H, Arai Y. Primary bone tumours. In: Imaging of the Sternocostoclavicular Region. Germany: Springer, Berlin, Heidelberg; 2007. p. 207-28.
Kadu VV, Saindane KA, Goghate N, Goghate N. Osteochondroma of the rib: A rare radiological apeareance. J Orthop Case Rep 2015;5:62-4.
Phatak SV, Kolwadkar PK, Rajderkar D. Solitary osteochondroma of rib: A case report. Indian J Radiol Imaging 2006;16:339. [Full text]
Maeda K, Watanabe T, Sato K, Takezoe T, Migita M, Takahashi M, et al
. Two cases of asymptomatic rib exostosis treated by prophylactic surgical excision. J Pediatr Surg Case Rep 2017;20:24-8.
Bess RS, Robbin MR, Bohlman HH, Thompson GH. Spinal exostoses: Analysis of twelve cases and review of the literature. Spine (Phila Pa 1976) 2005;30:774-80.
Naidu MC, Rao SS, Krishna CV, Rao S, Kumar PA. Costal osteochondroma of rib: Case report. J Evid Based Med Healthc 2015;2:2624-27.
Quirini GE, Meyer JR, Herman M, Russell EJ. Osteochondroma of the thoracic spine: An unusual cause of spinal cord compression. AJNR Am J Neuroradiol 1996;17:961-4.
Lee CY, Ham SY, Oh YW, Lee SH, Kim KT. Osteochondroma arising from a rib mimicking a calcifying anterior mediastinal mass. J Korean Radiol Soc 2007;57:533-5.
[Figure 1], [Figure 2], [Figure 3]