Lung India

CASE LETTER
Year
: 2020  |  Volume : 37  |  Issue : 3  |  Page : 277--279

Rare intrathoracic rib: Significance and associations in and adult


Arzu Canan1, Sachin S Saboo2, Kiran Batra1,  
1 Department of Radiology, University of Texas Southwestern Medical Center, Dallas, Texas, USA
2 Department of Radiology, University of Texas Health San Antonio, San Antonio, Texas, USA

Correspondence Address:
Arzu Canan
Department of Radiology, University of Texas Southwestern Medical Center, Dallas, Texas
USA




How to cite this article:
Canan A, Saboo SS, Batra K. Rare intrathoracic rib: Significance and associations in and adult.Lung India 2020;37:277-279


How to cite this URL:
Canan A, Saboo SS, Batra K. Rare intrathoracic rib: Significance and associations in and adult. Lung India [serial online] 2020 [cited 2020 Jul 4 ];37:277-279
Available from: http://www.lungindia.com/text.asp?2020/37/3/277/283749


Full Text



Intrathoracic rib is rarely encountered congenital abnormality of the thoracic rib cage. As it usually does not cause any clinical symptoms, the incidental demonstration might cause unnecessary further evaluation or misdiagnosis. We present multidetector computed tomography (MDCT) features of an incidentally detected supernumerary intrathoracic rib and its associated findings to increase the awareness and significance of this uncommon entity.

A 43-year-old female with a recent diagnosis of endometrioid carcinoma of the uterus was evaluated for the presence of metastasis. Physical examination of the respiratory system was unremarkable. The patient did not report any respiratory symptoms, smoking history, or prior thoracic surgery. Contrast-enhanced chest MDCT was performed, and multiplanar and three-dimensional reconstructions of the chest were created. No lung parenchymal or intrathoracic lymph nodal or osseous metastases were detected. Incidental note was made of a supernumerary intrathoracic corticated osseous rib originating from the proximal part and head of the right posterior fifth rib and extending inward and inferiorly along the posterior costal surface of the right hemithorax [Figure 1]. An additional small thin vertically projecting bony styloid-like process from the inferior edge of the proximal part of this supernumerary rib was present [Figure 2]a and [Figure 2]b. Associated findings included mild levoscoliosis of the thoracic spine, asymmetric enlargement of the head of the right fifth rib [Figure 3]a, excessive focal extrapleural fat tissue between the supernumerary rib and rib cage [Figure 3]b, and triangular soft-tissue density tissue suggestive of fibrous bands extending caudally from the inferior margin of the supernumerary rib to the posterior right hemidiaphragm [Figure 3]c. Moreover, anomalous drainage of the left superior pulmonary vein to the left innominate vein creating a left-to-right shunt was detected [Figure 4]a,[Figure 4]b,[Figure 4]c. Our patient was conservatively managed for this rib finding and associated intrathoracic abnormalities.{Figure 1}{Figure 2}{Figure 3}{Figure 4}

Supernumerary intrathoracic ribs are rare congenital abnormalities of the rib cage caused by fusion abnormalities of the sclerotomes in the embryologic life.[1] Less than fifty case reports have been published in the literature about intrathoracic rib since its first detection in 1947.[2] It is usually demonstrated on the right side and arises between the third and eighth ribs with no gender predilection.[3] Scoliosis is the only associated skeletal deformity with intrathoracic ribs as per the previous studies.[3],[4]

Kamano et al. had suggested a classification system including four different types depending on the location and course of the intrathoracic rib.[5] Type I intrathoracic rib represents the supernumerary rib originating from the vertebral body (Ia) or proximal part of the rib (Ib). Type II is also named as a bifid rib caused by a supernumerary rib extending from the distal part of the normal rib. Type III is not an actual supernumerary rib and is caused by a locally depressed rib. Finally, Type IV is a combination of Type II and III. According to this classification, our patient demonstrated the features of both Type Ib and Type II intrathoracic rib that was previously reported only in one case in the literature.[4]

The fibrous attachment to the diaphragmatic or mediastinal pleural surface causing pleural tenting or diaphragm elevation has been previously described in only a few cases.[6],[7],[8] Similarly, in our case, a fibrous tissue connecting supernumerary rib and posterior diaphragm was detected, which resulted in the pleural tenting and elevation of the right hemidiaphragm.

In brief, this case report reveals the unique appearance of the intrathoracic osseous rib and its associated findings of fibrous attachment to pleura and scoliosis. The new finding of partial anomalous pulmonary venous return in our patient could be an additional association or an incidental finding. Hence, paying careful attention and acknowledgment of these findings on computed tomography scan is required to avoid unnecessary investigations and ensure appropriate management.

This is a rare case of incidental intrathoracic rib and its associated findings in an adult woman. Although it does not cause any worrisome symptoms, the detection and radiological diagnosis of the intrathoracic rib and its associated findings might prevent unnecessary further evaluation and procedures.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

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